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leflunomide
leflunomide - 66993-160-30 - (leflunomide)
Drug Information of leflunomide
| Product NDC: | 66993-160 |
| Proprietary Name: | leflunomide |
| Non Proprietary Name: | leflunomide |
| Active Ingredient(s): | 10 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: | 66993-160 |
| Labeler Name: | Prasco LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020905 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19980910 |
Package Information of leflunomide
| Package NDC: | 66993-160-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (66993-160-30) |
NDC Information of leflunomide
| NDC Code | 66993-160-30 |
| Proprietary Name | leflunomide |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (66993-160-30) |
| Product NDC | 66993-160 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | leflunomide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19980910 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Prasco LLC |
| Substance Name | LEFLUNOMIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antirheumatic Agent [EPC] |
