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Amantadine Hydrochloride - 0781-2048-05 - (Amantadine Hydrochloride)

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Drug Information of Amantadine Hydrochloride

Product NDC: 0781-2048
Proprietary Name: Amantadine Hydrochloride
Non Proprietary Name: Amantadine Hydrochloride
Active Ingredient(s): 100    mg/1 & nbsp;   Amantadine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Amantadine Hydrochloride

Product NDC: 0781-2048
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071293
Marketing Category: ANDA
Start Marketing Date: 19870218

Package Information of Amantadine Hydrochloride

Package NDC: 0781-2048-05
Package Description: 500 CAPSULE in 1 BOTTLE (0781-2048-05)

NDC Information of Amantadine Hydrochloride

NDC Code 0781-2048-05
Proprietary Name Amantadine Hydrochloride
Package Description 500 CAPSULE in 1 BOTTLE (0781-2048-05)
Product NDC 0781-2048
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amantadine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19870218
Marketing Category Name ANDA
Labeler Name Sandoz 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 Hydrochloride


General Information