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Flumadine
Flumadine - 49708-521-88 - (flumadine)
Drug Information of Flumadine
| Product NDC: | 49708-521 |
| Proprietary Name: | Flumadine |
| Non Proprietary Name: | flumadine |
| Active Ingredient(s): | 100 mg/1 & nbsp; flumadine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flumadine
| Product NDC: | 49708-521 |
| Labeler Name: | Caraco Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019649 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090922 |
Package Information of Flumadine
| Package NDC: | 49708-521-88 |
| Package Description: | 100 TABLET in 1 BOTTLE (49708-521-88) |
NDC Information of Flumadine
| NDC Code | 49708-521-88 |
| Proprietary Name | Flumadine |
| Package Description | 100 TABLET in 1 BOTTLE (49708-521-88) |
| Product NDC | 49708-521 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | flumadine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090922 |
| Marketing Category Name | NDA |
| Labeler Name | Caraco Pharma, Inc. |
| Substance Name | RIMANTADINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA] |
