Methotrexate
- Product NDC
- 72162-2174
- 11-digit product format
- 721622174
- Labeler code
- 72162
- Product ID
- 72162-2174_2a3d5064-e336-459f-b0dc-28e50256b32e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methotrexate Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201749
- Marketing category
- ANDA
- Marketing start
- 2017-11-10
- Substance
- METHOTREXATE SODIUM
- 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 SODIUM | 2.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3IG1E710ZN |
| Rxcui | 105585 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2174-1 | Methotrexate | 100 in 1 BOTTLE | TABLET | 100 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2174 | METHOTREXATE (METHOTREXATE SODIUM) TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20231212_c7592288-ac24-46c6-8cec-9abe23d7e81e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2174-1 | 72162217401 | 100 TABLET in 1 BOTTLE (72162-2174-1) | 100 tablet | 2023-12-07 | No | No | Current |