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Amantadine Hydrochloride - 0832-0111-00 - (amantadine hydrochloride)

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Drug Information of Amantadine Hydrochloride

Product NDC: 0832-0111
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): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Amantadine Hydrochloride

Product NDC: 0832-0111
Labeler Name: Upsher-Smith Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076186
Marketing Category: ANDA
Start Marketing Date: 20111215

Package Information of Amantadine Hydrochloride

Package NDC: 0832-0111-00
Package Description: 100 TABLET in 1 BOTTLE (0832-0111-00)

NDC Information of Amantadine Hydrochloride

NDC Code 0832-0111-00
Proprietary Name Amantadine Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (0832-0111-00)
Product NDC 0832-0111
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amantadine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111215
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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