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Amantadine Hydrochloride - 55289-012-10 - (amantadine hydrochloride)

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Drug Information of Amantadine Hydrochloride

Product NDC: 55289-012
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, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Amantadine Hydrochloride

Product NDC: 55289-012
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070589
Marketing Category: ANDA
Start Marketing Date: 20110915

Package Information of Amantadine Hydrochloride

Package NDC: 55289-012-10
Package Description: 10 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (55289-012-10)

NDC Information of Amantadine Hydrochloride

NDC Code 55289-012-10
Proprietary Name Amantadine Hydrochloride
Package Description 10 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (55289-012-10)
Product NDC 55289-012
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amantadine hydrochloride
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20110915
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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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