trexall

Generic: methotrexate

Labeler: teva women's health, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trexall
Generic Name methotrexate
Labeler teva women's health, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

methotrexate sodium 7.5 mg/1

Manufacturer
Teva Women's Health, Inc.

Identifiers & Regulatory

Product NDC 51285-367
Product ID 51285-367_6743bd6d-9c6b-4f43-b444-8faa4b5d5221
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040385
Listing Expiration 2026-12-31
Marketing Start 2001-05-03

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 51285367
Hyphenated Format 51285-367

Supplemental Identifiers

RxCUI
105586 283510 283511 283671 284592 284593 284594 284595
UPC
0351285367013 0351285366016 0351285369017
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 trexall (source: ndc)
Generic Name methotrexate (source: ndc)
Application Number ANDA040385 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (51285-367-01)
source: ndc

Packages (1)

51285-367-01 30 TABLET, FILM COATED in 1 BOTTLE (51285-367-01)

Ingredients (1)

methotrexate sodium (7.5 mg/1)

Linked Drug Pages (1)

Trexall ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6743bd6d-9c6b-4f43-b444-8faa4b5d5221", "openfda": {"upc": ["0351285367013", "0351285366016", "0351285369017"], "unii": ["3IG1E710ZN"], "rxcui": ["105586", "283510", "283511", "283671", "284592", "284593", "284594", "284595"], "spl_set_id": ["e942f8db-510f-44d6-acb5-b822196f5e8c"], "manufacturer_name": ["Teva Women's Health, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51285-367-01)", "package_ndc": "51285-367-01", "marketing_start_date": "20010503"}], "brand_name": "Trexall", "product_id": "51285-367_6743bd6d-9c6b-4f43-b444-8faa4b5d5221", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "51285-367", "generic_name": "Methotrexate", "labeler_name": "Teva Women's Health, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trexall", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "7.5 mg/1"}], "application_number": "ANDA040385", "marketing_category": "ANDA", "marketing_start_date": "20010503", "listing_expiration_date": "20261231"}