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6505-01-110-3955

20 Products

NDC10223-0201-01

BENZOCAINE,BUTAMBEN,AND TETRACAINE HYDROCHLORIDE TOPICAL AEROSOL

NSN, MFG P/N

6505011103955

NSN

6505-01-110-3955

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NDC10223-0201-01

BENZOCAINE,BUTAMBEN,AND TETRACAINE HYDROCHLORIDE TOPICAL AEROSOL

NSN, MFG P/N

6505011103955

NSN

6505-01-110-3955

MFG

AMERISOURCEBERGEN DRUG CORPORATION DIV CORPORATE OFFICE

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.500 PERCENTAGE, W/V BENZALKONIUM CHLORIDE ACTIVE INGREDIENT AND 14.000 PERCENTAGE, W/V BENZOCAINE ACTIVE INGREDIENT AND 2.000 PERCENTAGE, W/V BUTAMBEN ACTIVE INGREDIENT AND 2.000 PERCENTAGE, W/V TETRACAINE HYDROCHLORIDE ACTIVE INGREDIENT AND 0.005
III PART NAME ASSIGNED BY CONTROLLING AGENCY: BENZOCAINE BUTAMBEN AND TETRACAINE HCL TOPICAL AEROSOL 56GM
PRIMARY CONTAINER CONTENT QUANTITY: 56.000 GRAMS
PRIMARY CONTAINER TYPE: BOTTLE, AEROSOL
SPECIAL FEATURES: IN ABLAND WATER SOLUABLE BASE; CONTAINS 0.50 PCT BENZALKONIUM CHLORIDE AND 0.05 PCT CETYL DIMETHYL ETHYL AMMONIUM BROMIDE AS PRESERVATIVES; WITH ONE DETACHABLE,STAINLESS STEEL CANNULA,WHICH,WHEN ATTACHED TO THE PROTRUDING PLASTIC TUBING ON THE
~1: BOTTLE,PERMITS ADMINISTRATION OF ANESTHETIC TO THE DESIRED SITE OF APPLICATION WHEN ACTIVATED
~1: PERCENTAGE W/V CETYL DIMETHYL ETHYL AMMONIUM BROMIDE ACTIVE INGREDIENT

2A0114

DEXTROSE INJECTION,USP

NSN, MFG P/N

6505011103956

NSN

6505-01-110-3956

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2A0114

DEXTROSE INJECTION,USP

NSN, MFG P/N

6505011103956

NSN

6505-01-110-3956

MFG

BAXTER HEALTHCARE CORP FENWAL DIV GOVERNMENT SALES LCII-03

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 70.000 PERCENTAGE, W/V DEXTROSE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DEXTROSE INJECTION USP 70% 500ML BT 6S
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: BOTTLE WITH A RATED CAPACITY OF NOT LESS THAN 1000 ML; THE STOPPER SHALL ACCEPT AND RETAIN THE PIERCING DEVICE OF STOCKLISTED INTRAVENOUS INJECTION SETS
TOTAL PRIMARY CONTAINER QUANTITY: 6

NDC00264-1129-01

DEXTROSE INJECTION,USP

NSN, MFG P/N

6505011103956

NSN

6505-01-110-3956

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NDC00264-1129-01

DEXTROSE INJECTION,USP

NSN, MFG P/N

6505011103956

NSN

6505-01-110-3956

MFG

B BRAUN MEDICAL INC WOUND CARE DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 70.000 PERCENTAGE, W/V DEXTROSE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DEXTROSE INJECTION USP 70% 500ML BT 6S
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: BOTTLE WITH A RATED CAPACITY OF NOT LESS THAN 1000 ML; THE STOPPER SHALL ACCEPT AND RETAIN THE PIERCING DEVICE OF STOCKLISTED INTRAVENOUS INJECTION SETS
TOTAL PRIMARY CONTAINER QUANTITY: 6

NDC00338-0033-13

DEXTROSE INJECTION,USP

NSN, MFG P/N

6505011103956

NSN

6505-01-110-3956

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NDC00338-0033-13

DEXTROSE INJECTION,USP

NSN, MFG P/N

6505011103956

NSN

6505-01-110-3956

MFG

BAXTER HEALTHCARE CORP IV SYSTEMS/GOV SALES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 70.000 PERCENTAGE, W/V DEXTROSE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DEXTROSE INJECTION USP 70% 500ML BT 6S
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: BOTTLE WITH A RATED CAPACITY OF NOT LESS THAN 1000 ML; THE STOPPER SHALL ACCEPT AND RETAIN THE PIERCING DEVICE OF STOCKLISTED INTRAVENOUS INJECTION SETS
TOTAL PRIMARY CONTAINER QUANTITY: 6

S1290-50

DEXTROSE INJECTION,USP

NSN, MFG P/N

6505011103956

NSN

6505-01-110-3956

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S1290-50

DEXTROSE INJECTION,USP

NSN, MFG P/N

6505011103956

NSN

6505-01-110-3956

MFG

B BRAUN MEDICAL INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 70.000 PERCENTAGE, W/V DEXTROSE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DEXTROSE INJECTION USP 70% 500ML BT 6S
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: BOTTLE WITH A RATED CAPACITY OF NOT LESS THAN 1000 ML; THE STOPPER SHALL ACCEPT AND RETAIN THE PIERCING DEVICE OF STOCKLISTED INTRAVENOUS INJECTION SETS
TOTAL PRIMARY CONTAINER QUANTITY: 6

NDC00054-3785-63

MORPHINE SULFATE ORAL SOLUTION

NSN, MFG P/N

6505011107196

NSN

6505-01-110-7196

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NDC00054-3785-63

MORPHINE SULFATE ORAL SOLUTION

NSN, MFG P/N

6505011107196

NSN

6505-01-110-7196

MFG

BOEHRINGER INGELHEIM ROXANE INC. DIV SUB OF BOEHRINGER INGELHEIM CORP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.000 MILLIGRAMS MORPHINE SULFATE PER MILLILITER
III CONTROLLED SUBSTANCE CLASSIFICATION: SCHEDULE II
III PART NAME ASSIGNED BY CONTROLLING AGENCY: MORPHINE SULFATE ORAL SOLUTION 10MG/5ML 500ML BT
III PROTECTIVE STORAGE FEATURE: VAULT STORAGE
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE

X1-490-352

VITAMIN A AND D OIN

NSN, MFG P/N

6505011109372

NSN

6505-01-110-9372

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X1-490-352

VITAMIN A AND D OIN

NSN, MFG P/N

6505011109372

NSN

6505-01-110-9372

MFG

PUBLIC HEALTH SERVICE

Description

GENERAL CHARACTERISTICS ITEM DESCRIPTION: 1 TUBE,EACH CONTAINING 2 OZ

NDC51079-0587-20

THIOTHIXENE CAPSULES,USP

NSN, MFG P/N

6505011109441

NSN

6505-01-110-9441

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NDC51079-0587-20

THIOTHIXENE CAPSULES,USP

NSN, MFG P/N

6505011109441

NSN

6505-01-110-9441

MFG

UDL LABORATORIES INC

Description

(NON-CORE DATA) UNIT PACKAGE TYPE: PACKAGE
ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.000 MILLIGRAMS THIOTHIXENE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
FEATURES PROVIDED: UNIT DOSE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: THIOTHIXENE CAPSULES USP 2MG 100S PG
PRIMARY CONTAINER TYPE: STRIP

18

LANOLIN,USP

NSN, MFG P/N

6505011109442

NSN

6505-01-110-9442

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18

LANOLIN,USP

NSN, MFG P/N

6505011109442

NSN

6505-01-110-9442

MFG

UNITED STATES PHARMACOPEIAL CONVENTION INC. THE DBA UNITED STATES PHARMACOPEIA

Description

PRIMARY CONTAINER CONTENT QUANTITY: 1.000 OUNCES
PRIMARY CONTAINER TYPE: TUBE, PLASTIC SQUEEZE
TOTAL PRIMARY CONTAINER QUANTITY: 1

MCKESSON CHEMICALS ALCOHOL

ALCOHOL,RUBBING,USP

NSN, MFG P/N

6505011109444

NSN

6505-01-110-9444

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MCKESSON CHEMICALS ALCOHOL

ALCOHOL,RUBBING,USP

NSN, MFG P/N

6505011109444

NSN

6505-01-110-9444

MFG

GENERAL SERVICES ADMINISTRATION FEDERAL SUPPLY SERVICE

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 99.000 PERCENTAGE, W/W ISOPROPYL ALCOHOL ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 1.000 GALLONS
PRIMARY CONTAINER TYPE: BOTTLE, PLASTIC

NDC00182-1919-89

CYCLOBENZAPRINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505011109926

NSN

6505-01-110-9926

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NDC00182-1919-89

CYCLOBENZAPRINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505011109926

NSN

6505-01-110-9926

MFG

IVAX CORP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS CYCLOBENZAPRINE HYDROCHLORIDE ACTIVE INGREDIENT
FEATURES PROVIDED: UNIT DOSE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CYCLOBENZAPRINE HYDROCHLORIDE TABLETS USP 10MG 100S PG
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: STRIP
PROTECTIVE STORAGE FEATURE: EXPIRATION DATED
TOTAL PRIMARY CONTAINER QUANTITY: 1

NDC51079-0644-20

CYCLOBENZAPRINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505011109926

NSN

6505-01-110-9926

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NDC51079-0644-20

CYCLOBENZAPRINE HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505011109926

NSN

6505-01-110-9926

MFG

UDL LABORATORIES INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 MILLIGRAMS CYCLOBENZAPRINE HYDROCHLORIDE ACTIVE INGREDIENT
FEATURES PROVIDED: UNIT DOSE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CYCLOBENZAPRINE HYDROCHLORIDE TABLETS USP 10MG 100S PG
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: STRIP
PROTECTIVE STORAGE FEATURE: EXPIRATION DATED
TOTAL PRIMARY CONTAINER QUANTITY: 1

DILANTIN

PHENYTOIN ORAL SUSPENSION,USP

NSN, MFG P/N

6505011112108

NSN

6505-01-111-2108

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DILANTIN

PHENYTOIN ORAL SUSPENSION,USP

NSN, MFG P/N

6505011112108

NSN

6505-01-111-2108

MFG

PARKE-DAVIS DIV OF WARNER-LAMBERT CO

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 125.000 MILLIGRAMS PHENYTOIN PER 5 MILLILITERS
FEATURES PROVIDED: UNIT DOSE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PHENYTION ORAL SUSPENSION USP 5ML POUCH 100S
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: POUCH, FOIL LAMINATE
TOTAL PRIMARY CONTAINER QUANTITY: 100

DILANTIN-125

PHENYTOIN ORAL SUSPENSION,USP

NSN, MFG P/N

6505011112108

NSN

6505-01-111-2108

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DILANTIN-125

PHENYTOIN ORAL SUSPENSION,USP

NSN, MFG P/N

6505011112108

NSN

6505-01-111-2108

MFG

PARKE-DAVIS DIV OF WARNER-LAMBERT CO

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 125.000 MILLIGRAMS PHENYTOIN PER 5 MILLILITERS
FEATURES PROVIDED: UNIT DOSE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PHENYTION ORAL SUSPENSION USP 5ML POUCH 100S
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: POUCH, FOIL LAMINATE
TOTAL PRIMARY CONTAINER QUANTITY: 100

NDC00071-2214-40

PHENYTOIN ORAL SUSPENSION,USP

NSN, MFG P/N

6505011112108

NSN

6505-01-111-2108

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NDC00071-2214-40

PHENYTOIN ORAL SUSPENSION,USP

NSN, MFG P/N

6505011112108

NSN

6505-01-111-2108

MFG

PARKE-DAVIS DIV OF WARNER-LAMBERT CO

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 125.000 MILLIGRAMS PHENYTOIN PER 5 MILLILITERS
FEATURES PROVIDED: UNIT DOSE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PHENYTION ORAL SUSPENSION USP 5ML POUCH 100S
PRIMARY CONTAINER CONTENT QUANTITY: 5.000 MILLILITERS
PRIMARY CONTAINER TYPE: POUCH, FOIL LAMINATE
TOTAL PRIMARY CONTAINER QUANTITY: 100

NDC00364-2434-01

AMOXAPINE TABLETS,USP

NSN, MFG P/N

6505011113194

NSN

6505-01-111-3194

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NDC00364-2434-01

AMOXAPINE TABLETS,USP

NSN, MFG P/N

6505011113194

NSN

6505-01-111-3194

MFG

HENRY SCHEIN INC. DIV SPECIAL MARKETS / FEDERAL SALES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 100.000 MILLIGRAMS AMOXAPINE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMOXAPINE TABLETS 100MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00591-5715-01

AMOXAPINE TABLETS,USP

NSN, MFG P/N

6505011113194

NSN

6505-01-111-3194

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NDC00591-5715-01

AMOXAPINE TABLETS,USP

NSN, MFG P/N

6505011113194

NSN

6505-01-111-3194

MFG

WATSON LABS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 100.000 MILLIGRAMS AMOXAPINE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMOXAPINE TABLETS 100MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00364-2433-01

AMOXAPINE TABLETS,USP

NSN, MFG P/N

6505011113195

NSN

6505-01-111-3195

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NDC00364-2433-01

AMOXAPINE TABLETS,USP

NSN, MFG P/N

6505011113195

NSN

6505-01-111-3195

MFG

HENRY SCHEIN INC. DIV SPECIAL MARKETS / FEDERAL SALES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS AMOXAPINE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMOXAPINE TABLETS 50MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00591-5714-01

AMOXAPINE TABLETS,USP

NSN, MFG P/N

6505011113195

NSN

6505-01-111-3195

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NDC00591-5714-01

AMOXAPINE TABLETS,USP

NSN, MFG P/N

6505011113195

NSN

6505-01-111-3195

MFG

WATSON PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS AMOXAPINE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: AMOXAPINE TABLETS 50MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00364-7030-16

KAOLIN AND PECTIN SUSPENSION

NSN, MFG P/N

6505011115268

NSN

6505-01-111-5268

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NDC00364-7030-16

KAOLIN AND PECTIN SUSPENSION

NSN, MFG P/N

6505011115268

NSN

6505-01-111-5268

MFG

SCHEIN HENRY INC

Description

PRIMARY CONTAINER CONTENT QUANTITY: 16.000 FLUID OUNCES
PRIMARY CONTAINER TYPE: BOTTLE