methotrexate

Generic: methotrexate

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methotrexate
Generic Name methotrexate
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methotrexate sodium 2.5 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0555-0572
Product ID 0555-0572_c21629c1-6adf-4f56-9a95-a7ec698a2e6f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA081099
Listing Expiration 2026-12-31
Marketing Start 1990-11-01

Pharmacologic Class

Classes
folate analog metabolic inhibitor [epc] folic acid metabolism inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05550572
Hyphenated Format 0555-0572

Supplemental Identifiers

RxCUI
105585
UNII
3IG1E710ZN

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name methotrexate (source: ndc)
Generic Name methotrexate (source: ndc)
Application Number ANDA081099 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0555-0572-02)
  • 36 TABLET in 1 BOTTLE (0555-0572-35)
source: ndc

Packages (2)

0555-0572-02 100 TABLET in 1 BOTTLE (0555-0572-02) 0555-0572-35 36 TABLET in 1 BOTTLE (0555-0572-35)

Ingredients (1)

methotrexate sodium (2.5 mg/1)

Linked Drug Pages (1)

Methotrexate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c21629c1-6adf-4f56-9a95-a7ec698a2e6f", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["9b34b1d8-d125-41a2-9f6f-3fab67b573bd"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0555-0572-02)", "package_ndc": "0555-0572-02", "marketing_start_date": "19901101"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (0555-0572-35)", "package_ndc": "0555-0572-35", "marketing_start_date": "19901101"}], "brand_name": "Methotrexate", "product_id": "0555-0572_c21629c1-6adf-4f56-9a95-a7ec698a2e6f", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "0555-0572", "generic_name": "Methotrexate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA081099", "marketing_category": "ANDA", "marketing_start_date": "19901101", "listing_expiration_date": "20261231"}