Package 0254-2000-01

Brand: penicillamine

Generic: penicillamine
NDC Package

Package Facts

Identity

Package NDC 0254-2000-01
Digits Only 0254200001
Product NDC 0254-2000
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0254-2000-01)

Marketing

Marketing Status
Marketed Since 2020-01-02
Brand penicillamine
Generic penicillamine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fef4bc4f-65a5-42ae-89fb-64815448a62c", "openfda": {"nui": ["N0000175713"], "upc": ["0302542000013"], "unii": ["GNN1DV99GX"], "rxcui": ["198071"], "spl_set_id": ["72ee469c-f9ef-4bb4-922f-5d71276664a5"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0254-2000-01)", "package_ndc": "0254-2000-01", "marketing_start_date": "20200102"}], "brand_name": "penicillamine", "product_id": "0254-2000_fef4bc4f-65a5-42ae-89fb-64815448a62c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "0254-2000", "generic_name": "penicillamine", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "penicillamine", "active_ingredients": [{"name": "PENICILLAMINE", "strength": "250 mg/1"}], "application_number": "ANDA211196", "marketing_category": "ANDA", "marketing_start_date": "20200102", "listing_expiration_date": "20261231"}