Package 46708-730-36

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 46708-730-36
Digits Only 4670873036
Product NDC 46708-730
Description

36 TABLET in 1 BOTTLE (46708-730-36)

Marketing

Marketing Status
Marketed Since 2024-06-04
Brand methotrexate
Generic methotrexate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ff55c573-dc84-4ff3-9d10-2b24c47dd679", "openfda": {"upc": ["0346708730369"], "unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["ff55c573-dc84-4ff3-9d10-2b24c47dd679"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (46708-730-31)", "package_ndc": "46708-730-31", "marketing_start_date": "20240604"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (46708-730-36)", "package_ndc": "46708-730-36", "marketing_start_date": "20240604"}], "brand_name": "METHOTREXATE", "product_id": "46708-730_ff55c573-dc84-4ff3-9d10-2b24c47dd679", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "46708-730", "generic_name": "METHOTREXATE", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHOTREXATE", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA217552", "marketing_category": "ANDA", "marketing_start_date": "20240604", "listing_expiration_date": "20261231"}