Package 68475-201-01

Brand: penicillamine

Generic: penicillamine
NDC Package

Package Facts

Identity

Package NDC 68475-201-01
Digits Only 6847520101
Product NDC 68475-201
Description

100 CAPSULE in 1 BOTTLE (68475-201-01)

Marketing

Marketing Status
Marketed Since 2022-01-01
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": "0ee5ea02-a892-408f-aa5d-42ab034bdfc4", "openfda": {"nui": ["N0000175713"], "unii": ["GNN1DV99GX"], "rxcui": ["198070"], "spl_set_id": ["064fb48d-aa34-4e52-9295-10f2ca4c77dc"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Navinta LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68475-201-01)", "package_ndc": "68475-201-01", "marketing_start_date": "20220101"}], "brand_name": "Penicillamine", "product_id": "68475-201_0ee5ea02-a892-408f-aa5d-42ab034bdfc4", "dosage_form": "CAPSULE", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "68475-201", "generic_name": "Penicillamine", "labeler_name": "Navinta LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Penicillamine", "active_ingredients": [{"name": "PENICILLAMINE", "strength": "250 mg/1"}], "application_number": "ANDA214363", "marketing_category": "ANDA", "marketing_start_date": "20220101", "listing_expiration_date": "20261231"}