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6505-01-239-5492

20 Products

NDC63323-0412-10

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012395492

NSN

6505-01-239-5492

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NDC63323-0412-10

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012395492

NSN

6505-01-239-5492

MFG

APP PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 MILLIGRAMS MIDAZOLAM EQUIVALENT PER MILLILITER
III CONTROLLED SUBSTANCE CLASSIFICATION: SCHEDULE IV
III PART NAME ASSIGNED BY CONTROLLING AGENCY: MIDAZOLAM HYDROCHLORIDE INJECTION 5MG/ML 10ML VIAL 10S
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, MULTIPLE DOSE
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC10019-0027-10

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012395492

NSN

6505-01-239-5492

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NDC10019-0027-10

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012395492

NSN

6505-01-239-5492

MFG

BAXTER HEALTHCARE CORPORATION DIV MEDICATION DELIVERY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 MILLIGRAMS MIDAZOLAM EQUIVALENT PER MILLILITER
III CONTROLLED SUBSTANCE CLASSIFICATION: SCHEDULE IV
III PART NAME ASSIGNED BY CONTROLLING AGENCY: MIDAZOLAM HYDROCHLORIDE INJECTION 5MG/ML 10ML VIAL 10S
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, MULTIPLE DOSE
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC53390-0126-10

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012395492

NSN

6505-01-239-5492

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NDC53390-0126-10

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012395492

NSN

6505-01-239-5492

MFG

VETERANS HEALTH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 MILLIGRAMS MIDAZOLAM EQUIVALENT PER MILLILITER
III CONTROLLED SUBSTANCE CLASSIFICATION: SCHEDULE IV
III PART NAME ASSIGNED BY CONTROLLING AGENCY: MIDAZOLAM HYDROCHLORIDE INJECTION 5MG/ML 10ML VIAL 10S
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, MULTIPLE DOSE
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC55390-0126-10

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012395492

NSN

6505-01-239-5492

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NDC55390-0126-10

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012395492

NSN

6505-01-239-5492

MFG

BEN VENUE LABORATORIES INC DBA BEDFORD LABORATORIES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 MILLIGRAMS MIDAZOLAM EQUIVALENT PER MILLILITER
III CONTROLLED SUBSTANCE CLASSIFICATION: SCHEDULE IV
III PART NAME ASSIGNED BY CONTROLLING AGENCY: MIDAZOLAM HYDROCHLORIDE INJECTION 5MG/ML 10ML VIAL 10S
PRIMARY CONTAINER CONTENT QUANTITY: 10.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, MULTIPLE DOSE
TOTAL PRIMARY CONTAINER QUANTITY: 10

5505-042

IOXAGLATE MEGLUMINE AND IOXAGLATE SODIUM,USP

NSN, MFG P/N

6505012396931

NSN

6505-01-239-6931

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5505-042

IOXAGLATE MEGLUMINE AND IOXAGLATE SODIUM,USP

NSN, MFG P/N

6505012396931

NSN

6505-01-239-6931

MFG

MALLINCKRODT INC ANESTHESIA PRODUCTS

Description

ADMINISTRATION: INTRA-ARTERIAL AND INTRAVENOUS
PRIMARY CONTAINER CONTENT QUANTITY: 30.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: EACH VIAL CONTAINS IOXAGLATE MEGLUMINE 39.3% AND IOXAGLATE SODIUM 19.6%; STERILE
TOTAL PRIMARY CONTAINER QUANTITY: 25

HEXABRIX

IOXAGLATE MEGLUMINE AND IOXAGLATE SODIUM,USP

NSN, MFG P/N

6505012396931

NSN

6505-01-239-6931

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HEXABRIX

IOXAGLATE MEGLUMINE AND IOXAGLATE SODIUM,USP

NSN, MFG P/N

6505012396931

NSN

6505-01-239-6931

MFG

MALLINCKRODT INC ANESTHESIA PRODUCTS

Description

ADMINISTRATION: INTRA-ARTERIAL AND INTRAVENOUS
PRIMARY CONTAINER CONTENT QUANTITY: 30.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: EACH VIAL CONTAINS IOXAGLATE MEGLUMINE 39.3% AND IOXAGLATE SODIUM 19.6%; STERILE
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC00019-5505-04

IOXAGLATE MEGLUMINE AND IOXAGLATE SODIUM,USP

NSN, MFG P/N

6505012396931

NSN

6505-01-239-6931

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NDC00019-5505-04

IOXAGLATE MEGLUMINE AND IOXAGLATE SODIUM,USP

NSN, MFG P/N

6505012396931

NSN

6505-01-239-6931

MFG

MALLINCKRODT INC ANESTHESIA PRODUCTS

Description

ADMINISTRATION: INTRA-ARTERIAL AND INTRAVENOUS
PRIMARY CONTAINER CONTENT QUANTITY: 30.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: EACH VIAL CONTAINS IOXAGLATE MEGLUMINE 39.3% AND IOXAGLATE SODIUM 19.6%; STERILE
TOTAL PRIMARY CONTAINER QUANTITY: 25

3154-96

VANCOMYCIN HYDROCHLORIDE,STERILE,USP

NSN, MFG P/N

6505012396933

NSN

6505-01-239-6933

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3154-96

VANCOMYCIN HYDROCHLORIDE,STERILE,USP

NSN, MFG P/N

6505012396933

NSN

6505-01-239-6933

MFG

AMERICAN CYANAMID CO LEDERLE LABORATORIES DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS VANCOMYCIN EQUIVALENT
ADMINISTRATION: INTRAVENOUS OR ORAL
FEATURES PROVIDED: STERILE
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLIGRAMS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: SINGLE DOSE VIAL; TO BE RECONSTITUTED WITH STERILE WATER FOR INTRAVENOUS USE AND WITH TAP WATER FOR ORAL USE;CAN DRINK IN JUICE OR STRAIGHT FROM THE VIAL

NDC00205-3154-96

VANCOMYCIN HYDROCHLORIDE,STERILE,USP

NSN, MFG P/N

6505012396933

NSN

6505-01-239-6933

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NDC00205-3154-96

VANCOMYCIN HYDROCHLORIDE,STERILE,USP

NSN, MFG P/N

6505012396933

NSN

6505-01-239-6933

MFG

AMERICAN CYANAMID CO LEDERLE LABORATORIES DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS VANCOMYCIN EQUIVALENT
ADMINISTRATION: INTRAVENOUS OR ORAL
FEATURES PROVIDED: STERILE
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLIGRAMS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: SINGLE DOSE VIAL; TO BE RECONSTITUTED WITH STERILE WATER FOR INTRAVENOUS USE AND WITH TAP WATER FOR ORAL USE;CAN DRINK IN JUICE OR STRAIGHT FROM THE VIAL

VANCOLED

VANCOMYCIN HYDROCHLORIDE,STERILE,USP

NSN, MFG P/N

6505012396933

NSN

6505-01-239-6933

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VANCOLED

VANCOMYCIN HYDROCHLORIDE,STERILE,USP

NSN, MFG P/N

6505012396933

NSN

6505-01-239-6933

MFG

AMERICAN CYANAMID CO LEDERLE LABORATORIES DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS VANCOMYCIN EQUIVALENT
ADMINISTRATION: INTRAVENOUS OR ORAL
FEATURES PROVIDED: STERILE
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLIGRAMS
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: SINGLE DOSE VIAL; TO BE RECONSTITUTED WITH STERILE WATER FOR INTRAVENOUS USE AND WITH TAP WATER FOR ORAL USE;CAN DRINK IN JUICE OR STRAIGHT FROM THE VIAL

301490734025

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

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301490734025

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

MFG

ANSPEC PTY LTD

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS DANTROLENE SODIUM ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DANTROLENE SODIUM FOR INJECTION 20 MG VIAL 6S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 20 MILLIGRAMS ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: CONTAINS 3000 MG MANNITOL AND SUFFICIENT SODIUM HYDROXIDE TO YIELD A PH OF APPROXIMATELY 9.5; FOR RECONSTITUTION W/WATER FOR INJECTION USP W/O BATERIOSTATIC AGENT; AVAIL THRU AMERISOURCE BERGEN IN PG OF "10'S", AVAIL THRU CARDINAL IN "1'S", ORDER
TOTAL PRIMARY CONTAINER QUANTITY: 6
~1: APPROPRIATELY

9315430053306

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

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9315430053306

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

MFG

GS1 AUSTRALIA PTY LTD

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS DANTROLENE SODIUM ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DANTROLENE SODIUM FOR INJECTION 20 MG VIAL 6S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 20 MILLIGRAMS ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: CONTAINS 3000 MG MANNITOL AND SUFFICIENT SODIUM HYDROXIDE TO YIELD A PH OF APPROXIMATELY 9.5; FOR RECONSTITUTION W/WATER FOR INJECTION USP W/O BATERIOSTATIC AGENT; AVAIL THRU AMERISOURCE BERGEN IN PG OF "10'S", AVAIL THRU CARDINAL IN "1'S", ORDER
TOTAL PRIMARY CONTAINER QUANTITY: 6
~1: APPROPRIATELY

DANTRIUM AMP 20 MG 6 X 2

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

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DANTRIUM AMP 20 MG 6 X 2

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

MFG

ANSPEC PTY LTD

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS DANTROLENE SODIUM ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DANTROLENE SODIUM FOR INJECTION 20 MG VIAL 6S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 20 MILLIGRAMS ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: CONTAINS 3000 MG MANNITOL AND SUFFICIENT SODIUM HYDROXIDE TO YIELD A PH OF APPROXIMATELY 9.5; FOR RECONSTITUTION W/WATER FOR INJECTION USP W/O BATERIOSTATIC AGENT; AVAIL THRU AMERISOURCE BERGEN IN PG OF "10'S", AVAIL THRU CARDINAL IN "1'S", ORDER
TOTAL PRIMARY CONTAINER QUANTITY: 6
~1: APPROPRIATELY

DANTRIUM I.V.

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

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DANTRIUM I.V.

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

MFG

PROCTER & GAMBLE PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS DANTROLENE SODIUM ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DANTROLENE SODIUM FOR INJECTION 20 MG VIAL 6S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 20 MILLIGRAMS ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: CONTAINS 3000 MG MANNITOL AND SUFFICIENT SODIUM HYDROXIDE TO YIELD A PH OF APPROXIMATELY 9.5; FOR RECONSTITUTION W/WATER FOR INJECTION USP W/O BATERIOSTATIC AGENT; AVAIL THRU AMERISOURCE BERGEN IN PG OF "10'S", AVAIL THRU CARDINAL IN "1'S", ORDER
TOTAL PRIMARY CONTAINER QUANTITY: 6
~1: APPROPRIATELY

DANTRIUM-IV

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

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DANTRIUM-IV

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

MFG

SIGMA PHARMACEUTICALS AUSTRALIA PTY LTD

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS DANTROLENE SODIUM ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DANTROLENE SODIUM FOR INJECTION 20 MG VIAL 6S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 20 MILLIGRAMS ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: CONTAINS 3000 MG MANNITOL AND SUFFICIENT SODIUM HYDROXIDE TO YIELD A PH OF APPROXIMATELY 9.5; FOR RECONSTITUTION W/WATER FOR INJECTION USP W/O BATERIOSTATIC AGENT; AVAIL THRU AMERISOURCE BERGEN IN PG OF "10'S", AVAIL THRU CARDINAL IN "1'S", ORDER
TOTAL PRIMARY CONTAINER QUANTITY: 6
~1: APPROPRIATELY

NDC00149-0734-02

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

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NDC00149-0734-02

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

MFG

JHP PHARMACEUTICALS LLC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS DANTROLENE SODIUM ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DANTROLENE SODIUM FOR INJECTION 20 MG VIAL 6S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 20 MILLIGRAMS ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: CONTAINS 3000 MG MANNITOL AND SUFFICIENT SODIUM HYDROXIDE TO YIELD A PH OF APPROXIMATELY 9.5; FOR RECONSTITUTION W/WATER FOR INJECTION USP W/O BATERIOSTATIC AGENT; AVAIL THRU AMERISOURCE BERGEN IN PG OF "10'S", AVAIL THRU CARDINAL IN "1'S", ORDER
TOTAL PRIMARY CONTAINER QUANTITY: 6
~1: APPROPRIATELY

NDC42023-0123-06

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

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NDC42023-0123-06

DANTROLENE SODIUM FOR INJECTION

NSN, MFG P/N

6505012396963

NSN

6505-01-239-6963

MFG

JHP PHARMACEUTICALS LLC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS DANTROLENE SODIUM ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DANTROLENE SODIUM FOR INJECTION 20 MG VIAL 6S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 20 MILLIGRAMS ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
SPECIAL FEATURES: CONTAINS 3000 MG MANNITOL AND SUFFICIENT SODIUM HYDROXIDE TO YIELD A PH OF APPROXIMATELY 9.5; FOR RECONSTITUTION W/WATER FOR INJECTION USP W/O BATERIOSTATIC AGENT; AVAIL THRU AMERISOURCE BERGEN IN PG OF "10'S", AVAIL THRU CARDINAL IN "1'S", ORDER
TOTAL PRIMARY CONTAINER QUANTITY: 6
~1: APPROPRIATELY

NDC00536-4124-10

PAPAVERINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES

NSN, MFG P/N

6505012399105

NSN

6505-01-239-9105

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NDC00536-4124-10

PAPAVERINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES

NSN, MFG P/N

6505012399105

NSN

6505-01-239-9105

MFG

RUGBY GROUP INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 150.000 MILLIGRAMS PAPAVERINE HYDROCHLORIDE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 1000.000
CAPSULE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER TYPE: BOTTLE
THERAPEUTIC EQUIVALENT: NOT LISTED

INDERAL

PROPRANOLOL HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505012399764

NSN

6505-01-239-9764

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INDERAL

PROPRANOLOL HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505012399764

NSN

6505-01-239-9764

MFG

WYETH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS PROPRANOLOL HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PROPRANOLOL HYDROCHLORIDE TABLETS USP 20 MG 5000S BT
PRIMARY CONTAINER CONTENT QUANTITY: 5000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00046-0422-95

PROPRANOLOL HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505012399764

NSN

6505-01-239-9764

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NDC00046-0422-95

PROPRANOLOL HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505012399764

NSN

6505-01-239-9764

MFG

WYETH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS PROPRANOLOL HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PROPRANOLOL HYDROCHLORIDE TABLETS USP 20 MG 5000S BT
PRIMARY CONTAINER CONTENT QUANTITY: 5000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE