Cimetidine - 0409-7445-01 - (CIMETIDINE HYDROCHLORIDE)

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Drug Information of Cimetidine

Product NDC: 0409-7445
Proprietary Name: Cimetidine
Non Proprietary Name: CIMETIDINE HYDROCHLORIDE
Active Ingredient(s): 150    mg/mL & nbsp;   CIMETIDINE HYDROCHLORIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cimetidine

Product NDC: 0409-7445
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074345
Marketing Category: ANDA
Start Marketing Date: 20110708

Package Information of Cimetidine

Package NDC: 0409-7445-01
Package Description: 10 VIAL, MULTI-DOSE in 1 CARTON (0409-7445-01) > 8 mL in 1 VIAL, MULTI-DOSE

NDC Information of Cimetidine

NDC Code 0409-7445-01
Proprietary Name Cimetidine
Package Description 10 VIAL, MULTI-DOSE in 1 CARTON (0409-7445-01) > 8 mL in 1 VIAL, MULTI-DOSE
Product NDC 0409-7445
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CIMETIDINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110708
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name CIMETIDINE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/mL
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Cimetidine


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