Package 51991-974-01

Brand: penicillamine

Generic: penicillamine
NDC Package

Package Facts

Identity

Package NDC 51991-974-01
Digits Only 5199197401
Product NDC 51991-974
Product ID 51991-974_704ba860-2350-4024-a2bb-fc379ea69218
Description

100 CAPSULE in 1 BOTTLE (51991-974-01)

Marketing

Marketing Status
Marketed Since 2021-11-12
Brand penicillamine
Generic penicillamine
Sample Package No

Linked Drug Pages (1)

Penicillamine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "704ba860-2350-4024-a2bb-fc379ea69218", "openfda": {"nui": ["N0000175713"], "upc": ["0351991974017"], "unii": ["GNN1DV99GX"], "rxcui": ["198070"], "spl_set_id": ["1320f46b-e243-4e93-b9c9-ad8eb7828de5"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Breckenridge Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (51991-974-01)", "package_ndc": "51991-974-01", "marketing_start_date": "20211112"}], "brand_name": "Penicillamine", "product_id": "51991-974_704ba860-2350-4024-a2bb-fc379ea69218", "dosage_form": "CAPSULE", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "51991-974", "generic_name": "Penicillamine", "labeler_name": "Breckenridge Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Penicillamine", "active_ingredients": [{"name": "PENICILLAMINE", "strength": "250 mg/1"}], "application_number": "ANDA215409", "marketing_category": "ANDA", "marketing_start_date": "20211112", "listing_expiration_date": "20261231"}