Package 48433-065-05

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 48433-065-05
Digits Only 4843306505
Product NDC 48433-065
Product ID 48433-065_49a1fdee-5587-e05a-e063-6294a90aebc5
Description

20 BLISTER PACK in 1 CARTON (48433-065-05) / 1 TABLET in 1 BLISTER PACK (48433-065-01)

Marketing

Marketing Status
Marketed Since 2026-01-19
Brand methotrexate
Generic methotrexate
Sample Package No

Linked Drug Pages (1)

Methotrexate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49a1fdee-5587-e05a-e063-6294a90aebc5", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["f177e6fa-c482-432d-8208-937468ab3f10"], "manufacturer_name": ["Safecor Health LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 CARTON (48433-065-05)  / 1 TABLET in 1 BLISTER PACK (48433-065-01)", "package_ndc": "48433-065-05", "marketing_start_date": "20260119"}], "brand_name": "Methotrexate", "product_id": "48433-065_49a1fdee-5587-e05a-e063-6294a90aebc5", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "48433-065", "generic_name": "methotrexate", "labeler_name": "Safecor Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA081235", "marketing_category": "ANDA", "marketing_start_date": "20260119", "listing_expiration_date": "20271231"}