Home > National Drug Code (NDC) > AMANTADINE HYDROCHLORIDE

AMANTADINE HYDROCHLORIDE - 0121-0646-16 - (AMANTADINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of AMANTADINE HYDROCHLORIDE

Product NDC: 0121-0646
Proprietary Name: AMANTADINE HYDROCHLORIDE
Non Proprietary Name: AMANTADINE HYDROCHLORIDE
Active Ingredient(s): 50    mg/5mL & nbsp;   AMANTADINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of AMANTADINE HYDROCHLORIDE

Product NDC: 0121-0646
Labeler Name: Pharmaceutical Associates, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074509
Marketing Category: ANDA
Start Marketing Date: 19950717

Package Information of AMANTADINE HYDROCHLORIDE

Package NDC: 0121-0646-16
Package Description: 473 mL in 1 BOTTLE (0121-0646-16)

NDC Information of AMANTADINE HYDROCHLORIDE

NDC Code 0121-0646-16
Proprietary Name AMANTADINE HYDROCHLORIDE
Package Description 473 mL in 1 BOTTLE (0121-0646-16)
Product NDC 0121-0646
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMANTADINE HYDROCHLORIDE
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19950717
Marketing Category Name ANDA
Labeler Name Pharmaceutical Associates, Inc.
Substance Name AMANTADINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/5mL
Pharmaceutical Classes Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]

Complete Information of AMANTADINE HYDROCHLORIDE


General Information