Methotrexate
- Product NDC
- 51079-570
- 11-digit product format
- 510790570
- Labeler code
- 51079
- Product ID
- 51079-570_e16f12a8-9abb-31a2-e053-2995a90a81b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methotrexate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA081235
- Marketing category
- ANDA
- Marketing start
- 1995-07-12
- Marketing end
- 2030-01-31
- Substance
- METHOTREXATE SODIUM
- Active strength
- 3 mg/1
- Pharmacologic classes
- Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51079-570-05 | 51079057005 | 20 BLISTER PACK in 1 CARTON (51079-570-05) > 1 TABLET in 1 BLISTER PACK (51079-570-01) | 20 blister pack | 1995-07-12 | 2030-01-31 | No | No | Current |