Package 0254-2000-01
Brand: penicillamine
Generic: penicillaminePackage 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
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"}