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Amantadine HCl - 10888-5006-3 - (AMANTADINE HYDROCHLORIDE)

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Drug Information of Amantadine HCl

Product NDC: 10888-5006
Proprietary Name: Amantadine HCl
Non Proprietary Name: AMANTADINE HYDROCHLORIDE
Active Ingredient(s): 100    mg/1 & nbsp;   AMANTADINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Amantadine HCl

Product NDC: 10888-5006
Labeler Name: Banner Pharmacaps Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078720
Marketing Category: ANDA
Start Marketing Date: 20121101

Package Information of Amantadine HCl

Package NDC: 10888-5006-3
Package Description: 500 CAPSULE, LIQUID FILLED in 1 BOTTLE (10888-5006-3)

NDC Information of Amantadine HCl

NDC Code 10888-5006-3
Proprietary Name Amantadine HCl
Package Description 500 CAPSULE, LIQUID FILLED in 1 BOTTLE (10888-5006-3)
Product NDC 10888-5006
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMANTADINE HYDROCHLORIDE
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20121101
Marketing Category Name ANDA
Labeler Name Banner Pharmacaps Inc
Substance Name AMANTADINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]

Complete Information of Amantadine HCl


General Information