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Amantadine Hydrochloride - 68084-611-01 - (Amantadine Hydrochloride)

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Drug Information of Amantadine Hydrochloride

Product NDC: 68084-611
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: 68084-611
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071293
Marketing Category: ANDA
Start Marketing Date: 20130117

Package Information of Amantadine Hydrochloride

Package NDC: 68084-611-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-611-01) > 10 CAPSULE in 1 BLISTER PACK (68084-611-11)

NDC Information of Amantadine Hydrochloride

NDC Code 68084-611-01
Proprietary Name Amantadine Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (68084-611-01) > 10 CAPSULE in 1 BLISTER PACK (68084-611-11)
Product NDC 68084-611
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amantadine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130117
Marketing Category Name ANDA
Labeler Name American Health Packaging
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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