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Leflunomide
Leflunomide - 0781-5057-31 - (Leflunomide)
Drug Information of Leflunomide
| Product NDC: | 0781-5057 |
| Proprietary Name: | Leflunomide |
| Non Proprietary Name: | Leflunomide |
| Active Ingredient(s): | 20 mg/1 & nbsp; Leflunomide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Leflunomide
| Product NDC: | 0781-5057 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077087 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050913 |
Package Information of Leflunomide
| Package NDC: | 0781-5057-31 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (0781-5057-31) |
NDC Information of Leflunomide
| NDC Code | 0781-5057-31 |
| Proprietary Name | Leflunomide |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0781-5057-31) |
| Product NDC | 0781-5057 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Leflunomide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20050913 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | LEFLUNOMIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antirheumatic Agent [EPC] |
