Methotrexate
- Product NDC
- 51079-570
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methotrexate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA081235
- Marketing category
- ANDA
- Substance
- METHOTREXATE SODIUM
- Current FDA listing
- Historical FDA.report record
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 51079-570-05 | 20 BLISTER PACK in 1 CARTON (51079-570-05) > 1 TABLET in 1 BLISTER PACK (51079-570-01) | 1995-07-12 | 2030-01-31 | No | Current |