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Amantadine Hydrochloride - 0527-1704-01 - (Amantadine Hydrochloride)

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Drug Information of Amantadine Hydrochloride

Product NDC: 0527-1704
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: 0527-1704
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078720
Marketing Category: ANDA
Start Marketing Date: 20081101

Package Information of Amantadine Hydrochloride

Package NDC: 0527-1704-01
Package Description: 100 CAPSULE in 1 BOTTLE (0527-1704-01)

NDC Information of Amantadine Hydrochloride

NDC Code 0527-1704-01
Proprietary Name Amantadine Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (0527-1704-01)
Product NDC 0527-1704
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amantadine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20081101
Marketing Category Name ANDA
Labeler Name Lannett Company, 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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