Methotrexate
- Product NDC
- 51407-121
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methotrexate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA081235
- Marketing category
- ANDA
- Substance
- METHOTREXATE SODIUM
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 51407-121-01 | 100 TABLET in 1 BOTTLE, PLASTIC (51407-121-01) | 2018-06-07 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| METHOTREXATE TABLETS. These highlights do not include all the information needed to use METHOTREXATE TABLETS safely and effectively. See full prescribing information for METHOTREXATE TABLETS. METHOTREXATE tablets, for oral use Initial U.S. Approval: 1953 | Golden State Medical Supply, Inc. | 2026-04-15 | HUMAN PRESCRIPTION DRUG LABEL | 10 |