Package 64850-330-01

Brand: methotrexate sodium

Generic: methotrexate sodium
NDC Package

Package Facts

Identity

Package NDC 64850-330-01
Digits Only 6485033001
Product NDC 64850-330
Product ID 64850-330_8dde104c-5e16-4d3b-93ae-2a464e033270
Description

100 TABLET in 1 BOTTLE, PLASTIC (64850-330-01)

Marketing

Marketing Status
Marketed Since 2024-05-16
Brand methotrexate sodium
Generic methotrexate sodium
Sample Package No

Linked Drug Pages (1)

Methotrexate Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8dde104c-5e16-4d3b-93ae-2a464e033270", "openfda": {"upc": ["0364850330015"], "unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["89c05ea3-3be1-46dd-b112-29c436fd7289"], "manufacturer_name": ["Elite Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (64850-330-01)", "package_ndc": "64850-330-01", "marketing_start_date": "20240516"}], "brand_name": "Methotrexate Sodium", "product_id": "64850-330_8dde104c-5e16-4d3b-93ae-2a464e033270", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "64850-330", "generic_name": "Methotrexate Sodium", "labeler_name": "Elite Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate Sodium", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA216453", "marketing_category": "ANDA", "marketing_start_date": "20240516", "listing_expiration_date": "20261231"}