Methotrexate
- Product NDC
- 69238-1423
- 11-digit product format
- 692381423
- Labeler code
- 69238
- Product ID
- 69238-1423_dc64275b-6b67-478c-992f-9d41f5cf4314
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methotrexate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals NY LLC
- Application
- ANDA210040
- Marketing category
- ANDA
- Marketing start
- 2017-12-29
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69238-1423 | METHOTREXATE TABLET [AMNEAL PHARMACEUTICALS NY LLC] | 11 | Legacy NDC | 20231231_dd39255b-81d1-4c08-aecf-acc4f2cdc04a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69238-1423-1 | 69238142301 | 100 TABLET in 1 BOTTLE (69238-1423-1) | 100 tablet | 2017-12-29 | 0000-00-00 | No | No | Current |
| 69238-1423-6 | 69238142306 | 36 TABLET in 1 BOTTLE (69238-1423-6) | 36 tablet | 2017-12-29 | 0000-00-00 | No | No | Current |