Methotrexate
- Product NDC
- 50090-3418
- 11-digit product format
- 500903418
- Labeler code
- 50090
- Product ID
- 50090-3418_712f6e3f-bd74-4cc0-bc02-aa70d8093f05
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methotrexate Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA201749
- Marketing category
- ANDA
- Marketing start
- 2017-11-10
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3418-2 | 50090341802 | 100 TABLET in 1 BOTTLE (50090-3418-2) | 100 tablet | 2018-03-26 | 0000-00-00 | No | No | Current |
| 50090-3418-9 | 50090341809 | 36 TABLET in 1 BOTTLE (50090-3418-9) | 36 tablet | 2018-05-02 | 0000-00-00 | No | No | Current |