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Amantadine Hydrochloride - 0832-2012-50 - (Amantadine Hydrochloride)

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Drug Information of Amantadine Hydrochloride

Product NDC: 0832-2012
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: 0832-2012
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071293
Marketing Category: ANDA
Start Marketing Date: 19870218

Package Information of Amantadine Hydrochloride

Package NDC: 0832-2012-50
Package Description: 500 CAPSULE in 1 BOTTLE (0832-2012-50)

NDC Information of Amantadine Hydrochloride

NDC Code 0832-2012-50
Proprietary Name Amantadine Hydrochloride
Package Description 500 CAPSULE in 1 BOTTLE (0832-2012-50)
Product NDC 0832-2012
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 Upsher-Smith Laboratories, 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


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