Methotrexate
- Product NDC
- 0904-7141
- 11-digit product format
- 009047141
- Labeler code
- 0904
- Product ID
- 0904-7141_f33af79d-4c98-45c6-a272-4e17a40fac3a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methotrexate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA207812
- Marketing category
- ANDA
- Marketing start
- 2017-02-09
- Substance
- METHOTREXATE
- Active strength
- 2.5 mg/1
- Pharmacologic classes
- Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Methotrexate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHOTREXATE | 2.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YL5FZ2Y5U1 |
| Rxcui | 105585 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0904-7141-10 | Methotrexate | 20 in 1 CARTON | TABLET | 20 | | 6 |
| 0904-7141-10 | Methotrexate | 1 in 1 BLISTER PACK | TABLET | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7141 | METHOTREXATE TABLET [MAJOR PHARMACEUTICALS] | 5 | Current NDC, Legacy NDC, 2 package rows | 20241115_2a6afc4c-819d-4ba9-8040-4504519c116a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7141-10 | 00904714110 | 20 BLISTER PACK in 1 CARTON (0904-7141-10) / 1 TABLET in 1 BLISTER PACK | 20 blister pack | 2017-02-09 | 0000-00-00 | No | No | Current |