Package 0378-0014-01

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 0378-0014-01
Digits Only 0378001401
Product NDC 0378-0014
Product ID 0378-0014_8088c399-5814-4d51-84fc-e95edd5751f5
Description

100 TABLET in 1 BOTTLE, PLASTIC (0378-0014-01)

Marketing

Marketing Status
Marketed Since 1992-05-18
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": "8088c399-5814-4d51-84fc-e95edd5751f5", "openfda": {"upc": ["0303780014015"], "unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["70c09984-2b36-424f-8b27-3fd0cd4e833d"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0378-0014-01)", "package_ndc": "0378-0014-01", "marketing_start_date": "19920518"}], "brand_name": "Methotrexate", "product_id": "0378-0014_8088c399-5814-4d51-84fc-e95edd5751f5", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "0378-0014", "generic_name": "methotrexate", "labeler_name": "Mylan Pharmaceuticals Inc.", "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": "19920518", "listing_expiration_date": "20261231"}