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Procainamide Hydrochloride - 55154-6986-8 - (PROCAINAMIDE HYDROCHLORIDE)

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Drug Information of Procainamide Hydrochloride

Product NDC: 55154-6986
Proprietary Name: Procainamide Hydrochloride
Non Proprietary Name: PROCAINAMIDE HYDROCHLORIDE
Active Ingredient(s): 100    mg/mL & nbsp;   PROCAINAMIDE HYDROCHLORIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Procainamide Hydrochloride

Product NDC: 55154-6986
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089069
Marketing Category: ANDA
Start Marketing Date: 20110708

Package Information of Procainamide Hydrochloride

Package NDC: 55154-6986-8
Package Description: 1 VIAL, MULTI-DOSE in 1 BAG (55154-6986-8) > 10 mL in 1 VIAL, MULTI-DOSE

NDC Information of Procainamide Hydrochloride

NDC Code 55154-6986-8
Proprietary Name Procainamide Hydrochloride
Package Description 1 VIAL, MULTI-DOSE in 1 BAG (55154-6986-8) > 10 mL in 1 VIAL, MULTI-DOSE
Product NDC 55154-6986
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PROCAINAMIDE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110708
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name PROCAINAMIDE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Antiarrhythmic [EPC]

Complete Information of Procainamide Hydrochloride


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