Package 47335-235-96

Brand: methotrexate

Generic: methotrexate sodium
NDC Package

Package Facts

Identity

Package NDC 47335-235-96
Digits Only 4733523596
Product NDC 47335-235
Product ID 47335-235_15524c15-09e2-4eb2-bba7-a5e51d8ead07
Description

36 TABLET in 1 BOTTLE (47335-235-96)

Marketing

Marketing Status
Marketed Since 2017-11-10
Brand methotrexate
Generic methotrexate sodium
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": "15524c15-09e2-4eb2-bba7-a5e51d8ead07", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["8f1260de-b60c-4f0e-8af6-0e957b0a281b"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (47335-235-83)", "package_ndc": "47335-235-83", "marketing_start_date": "20171110"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (47335-235-96)", "package_ndc": "47335-235-96", "marketing_start_date": "20171110"}], "brand_name": "Methotrexate", "product_id": "47335-235_15524c15-09e2-4eb2-bba7-a5e51d8ead07", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "47335-235", "generic_name": "Methotrexate Sodium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA201749", "marketing_category": "ANDA", "marketing_start_date": "20171110", "listing_expiration_date": "20261231"}