METHOTREXATE
- Product NDC
- 67253-320
- 11-digit product format
- 672530320
- Labeler code
- 67253
- Product ID
- 67253-320_cfc59348-8d35-482f-8afa-4e8cf303d813
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHOTREXATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- NDA008085
- Marketing category
- NDA
- Marketing start
- 1953-12-07
- Marketing end
- 2021-02-28
- 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 |
|---|
| 67253-320-10 | 67253032010 | 100 TABLET in 1 BOTTLE (67253-320-10) | 100 tablet | 1953-12-07 | 2021-02-28 | No | No | Current |
| 67253-320-36 | 67253032036 | 36 TABLET in 1 BOTTLE (67253-320-36) | 36 tablet | 1953-12-07 | 2021-02-28 | No | No | Current |