Package 62135-772-35

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 62135-772-35
Digits Only 6213577235
Product NDC 62135-772
Product ID 62135-772_462a5023-e5a1-692a-e063-6294a90a7236
Description

36 TABLET in 1 BOTTLE (62135-772-35)

Marketing

Marketing Status
Marketed Since 2023-08-29
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": "462a5023-e5a1-692a-e063-6294a90a7236", "openfda": {"upc": ["0362135772352"], "unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["2609da8f-80dc-448e-8eba-35d11488ce7f"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "36 TABLET in 1 BOTTLE (62135-772-35)", "package_ndc": "62135-772-35", "marketing_start_date": "20230829"}], "brand_name": "Methotrexate", "product_id": "62135-772_462a5023-e5a1-692a-e063-6294a90a7236", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "62135-772", "generic_name": "Methotrexate", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA210454", "marketing_category": "ANDA", "marketing_start_date": "20200130", "listing_expiration_date": "20261231"}