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Rimantadine Hydrochloride
Rimantadine Hydrochloride - 0115-1911-02 - (Rimantadine Hydrochloride)
Drug Information of Rimantadine Hydrochloride
| Product NDC: | 0115-1911 |
| Proprietary Name: | Rimantadine Hydrochloride |
| Non Proprietary Name: | Rimantadine Hydrochloride |
| Active Ingredient(s): | 100 mg/1 & nbsp; Rimantadine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rimantadine Hydrochloride
| Product NDC: | 0115-1911 |
| Labeler Name: | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076132 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050401 |
Package Information of Rimantadine Hydrochloride
| Package NDC: | 0115-1911-02 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE (0115-1911-02) |
NDC Information of Rimantadine Hydrochloride
| NDC Code | 0115-1911-02 |
| Proprietary Name | Rimantadine Hydrochloride |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (0115-1911-02) |
| Product NDC | 0115-1911 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Rimantadine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20050401 |
| Marketing Category Name | ANDA |
| Labeler Name | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
| Substance Name | RIMANTADINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA] |
