Package 0555-0572-02
Brand: methotrexate
Generic: methotrexatePackage Facts
Identity
Package NDC
0555-0572-02
Digits Only
0555057202
Product NDC
0555-0572
Description
100 TABLET in 1 BOTTLE (0555-0572-02)
Marketing
Marketing Status
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": "c21629c1-6adf-4f56-9a95-a7ec698a2e6f", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["9b34b1d8-d125-41a2-9f6f-3fab67b573bd"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0555-0572-02)", "package_ndc": "0555-0572-02", "marketing_start_date": "19901101"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (0555-0572-35)", "package_ndc": "0555-0572-35", "marketing_start_date": "19901101"}], "brand_name": "Methotrexate", "product_id": "0555-0572_c21629c1-6adf-4f56-9a95-a7ec698a2e6f", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "0555-0572", "generic_name": "Methotrexate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA081099", "marketing_category": "ANDA", "marketing_start_date": "19901101", "listing_expiration_date": "20261231"}