Product NDC: | 54569-0084 |
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) |
Product NDC: | 54569-0084 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA071293 |
Marketing Category: | ANDA |
Start Marketing Date: | 19870218 |
Package NDC: | 54569-0084-3 |
Package Description: | 10 CAPSULE in 1 BOTTLE (54569-0084-3) |
NDC Code | 54569-0084-3 |
Proprietary Name | Amantadine Hydrochloride |
Package Description | 10 CAPSULE in 1 BOTTLE (54569-0084-3) |
Product NDC | 54569-0084 |
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 | A-S Medication Solutions LLC |
Substance Name | AMANTADINE HYDROCHLORIDE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA] |