Adenosine (Page 3 of 3)

PRINCIPAL DISPLAY PANEL

Adenosine Injection, USP
6 mg/2 mL
(3 mg/mL)
2 mL Single Dose Vial
NDC 0641-6113-01

Adenosine Injection, USP 6 mg/2 mL (3 mg/mL) 2 mL Single Dose Vial

Adenosine Injection, USP
6 mg/2 mL
(3 mg/mL)
10 x 2 mL Single Dose Vials
NDC 0641-6113-10

Adenosine Injection, USP 6 mg/2 mL (3 mg/mL) 10 x 2 mL Single Dose Vials
(click image for full-size original)
ADENOSINE
adenosine injection
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0641-6113
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ADENOSINE (ADENOSINE) ADENOSINE 3 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE 9 mg in 1 mL
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0641-6113-10 10 VIAL in 1 CARTON contains a VIAL (0641-6113-01)
1 NDC:0641-6113-01 2 mL in 1 VIAL This package is contained within the CARTON (0641-6113-10)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076500 06/16/2004
Labeler — Hikma Pharmaceuticals USA Inc. (946499746)
Establishment
Name Address ID/FEI Operations
BAXTER PHARMACEUTICAL SOLUTIONS, LLC 604719430 ANALYSIS (0641-6113), LABEL (0641-6113), MANUFACTURE (0641-6113), PACK (0641-6113), STERILIZE (0641-6113)

Revised: 12/2019 Hikma Pharmaceuticals USA Inc.

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