| NDC Code | 68151-2103-0 |
|---|
| Package Description | 1 TABLET, FILM COATED in 1 PACKAGE (68151-2103-0) |
|---|
| Product NDC | 68151-2103 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Rimantadine Hydrochloride |
|---|
| Non-Proprietary Name | Rimantadine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20050401 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076132 |
|---|
| Manufacturer | Carilion Materials Management |
|---|
| Substance Name | RIMANTADINE HYDROCHLORIDE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA] |
|---|