methotrexate

Generic: methotrexate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methotrexate
Generic Name methotrexate
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methotrexate sodium 2.5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1772
Product ID 71335-1772_666230f1-6a5f-43cc-9e9c-7fdb2d8980fc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213343
Listing Expiration 2026-12-31
Marketing Start 2020-08-24

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 713351772
Hyphenated Format 71335-1772

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 ANDA213343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1772-1)
  • 12 TABLET in 1 BOTTLE (71335-1772-2)
  • 20 TABLET in 1 BOTTLE (71335-1772-3)
  • 100 TABLET in 1 BOTTLE (71335-1772-4)
  • 36 TABLET in 1 BOTTLE (71335-1772-5)
  • 24 TABLET in 1 BOTTLE (71335-1772-6)
  • 90 TABLET in 1 BOTTLE (71335-1772-7)
  • 4 TABLET in 1 BOTTLE (71335-1772-8)
source: ndc

Packages (8)

Ingredients (1)

methotrexate sodium (2.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "666230f1-6a5f-43cc-9e9c-7fdb2d8980fc", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["4741a44f-0d0b-4380-84f6-231a8d1560fb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1772-1)", "package_ndc": "71335-1772-1", "marketing_start_date": "20211229"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE (71335-1772-2)", "package_ndc": "71335-1772-2", "marketing_start_date": "20211229"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-1772-3)", "package_ndc": "71335-1772-3", "marketing_start_date": "20211229"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1772-4)", "package_ndc": "71335-1772-4", "marketing_start_date": "20211229"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (71335-1772-5)", "package_ndc": "71335-1772-5", "marketing_start_date": "20211229"}, {"sample": false, "description": "24 TABLET in 1 BOTTLE (71335-1772-6)", "package_ndc": "71335-1772-6", "marketing_start_date": "20210121"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1772-7)", "package_ndc": "71335-1772-7", "marketing_start_date": "20211229"}, {"sample": false, "description": "4 TABLET in 1 BOTTLE (71335-1772-8)", "package_ndc": "71335-1772-8", "marketing_start_date": "20211229"}], "brand_name": "Methotrexate", "product_id": "71335-1772_666230f1-6a5f-43cc-9e9c-7fdb2d8980fc", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "71335-1772", "generic_name": "Methotrexate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA213343", "marketing_category": "ANDA", "marketing_start_date": "20200824", "listing_expiration_date": "20261231"}