Methotrexate
- Product NDC
- 61703-408
- 11-digit product format
- 617030408
- Labeler code
- 61703
- Product ID
- 61703-408_37b3e76b-ac3d-4f93-adf1-91f52f676b8a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methotrexate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Hospira, Inc.
- Application
- NDA011719
- Marketing category
- NDA
- Marketing start
- 2013-11-11
- Substance
- METHOTREXATE SODIUM
- Active strength
- 25 mg/mL
- 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 | 25 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3IG1E710ZN |
| Rxcui | 1655956, 1946772 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61703-408-41 | Methotrexate | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 19 |
| 61703-408-41 | Methotrexate | 40 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 40 | | 19 |
| 61703-408-25 | Methotrexate | 40 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 40 | | 17 |
| 61703-408-25 | Methotrexate | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 17 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| METHOTREXATE SODIUM | ACTIVE INGREDIENT | 3IG1E710ZN | METHOTREXATE (METHOTREXATE SODIUM) INJECTION, SOLUTION [HOSPIRA WORLDWIDE, INC.] | 1 | |
| METHOTREXATE | ACTIVE MOIETY | YL5FZ2Y5U1 | METHOTREXATE (METHOTREXATE SODIUM) INJECTION, SOLUTION [HOSPIRA WORLDWIDE, INC.] | 1 | |
| BENZYL ALCOHOL | INACTIVE INGREDIENT | LKG8494WBH | METHOTREXATE (METHOTREXATE SODIUM) INJECTION, SOLUTION [HOSPIRA WORLDWIDE, INC.] | 1 | |
| HYDROCHLORIC ACID | INACTIVE INGREDIENT | QTT17582CB | METHOTREXATE (METHOTREXATE SODIUM) INJECTION, SOLUTION [HOSPIRA WORLDWIDE, INC.] | 1 | |
| SODIUM CHLORIDE | INACTIVE INGREDIENT | 451W47IQ8X | METHOTREXATE (METHOTREXATE SODIUM) INJECTION, SOLUTION [HOSPIRA WORLDWIDE, INC.] | 1 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | METHOTREXATE (METHOTREXATE SODIUM) INJECTION, SOLUTION [HOSPIRA WORLDWIDE, INC.] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | METHOTREXATE (METHOTREXATE SODIUM) INJECTION, SOLUTION [HOSPIRA WORLDWIDE, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61703-408 | METHOTREXATE INJECTION, SOLUTION [HOSPIRA, INC.] | 18 | Current NDC, Legacy NDC, 2 package rows | 20240829_0d63ba29-b692-41b4-87e8-351265c8273f.zip |
| 61703-408 | METHOTREXATE INJECTION, SOLUTION [HOSPIRA, INC.] | 15 | Current NDC, Legacy NDC, 2 package rows | 20240829_0e30eaef-5a09-4104-8a11-c32933eadeab.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61703-408-25 | 61703040825 | 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-408-25) / 40 mL in 1 VIAL, SINGLE-DOSE | 2013-11-11 | 0000-00-00 | No | No | Current |
| 61703-408-41 | 61703040841 | 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-408-41) / 40 mL in 1 VIAL, SINGLE-DOSE | 2001-02-26 | 0000-00-00 | No | No | Current |