methotrexate

Generic: methotrexate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methotrexate
Generic Name methotrexate
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methotrexate sodium 2.5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5457
Product ID 50090-5457_9a056178-22ac-4049-87ac-226d306eea2d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA081099
Listing Expiration 2027-12-31
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 500905457
Hyphenated Format 50090-5457

Supplemental Identifiers

RxCUI
105585
UNII
3IG1E710ZN

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
  • 36 TABLET in 1 BOTTLE (50090-5457-9)
source: ndc

Packages (1)

50090-5457-9 36 TABLET in 1 BOTTLE (50090-5457-9)

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": "9a056178-22ac-4049-87ac-226d306eea2d", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["22e10810-16fb-4c84-bccf-972405b77ef8"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "36 TABLET in 1 BOTTLE (50090-5457-9)", "package_ndc": "50090-5457-9", "marketing_start_date": "20210129"}], "brand_name": "Methotrexate", "product_id": "50090-5457_9a056178-22ac-4049-87ac-226d306eea2d", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "50090-5457", "generic_name": "Methotrexate", "labeler_name": "A-S Medication Solutions", "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": "20271231"}