Package 71205-916-00

Brand: penicillamine

Generic: penicillamine
NDC Package

Package Facts

Identity

Package NDC 71205-916-00
Digits Only 7120591600
Product NDC 71205-916
Description

100 CAPSULE in 1 BOTTLE (71205-916-00)

Marketing

Marketing Status
Marketed Since 2021-07-08
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": "125ca13e-9784-45be-847a-6fdf9875bd6a", "openfda": {"nui": ["N0000175713"], "upc": ["0371205916008"], "unii": ["GNN1DV99GX"], "rxcui": ["198070"], "spl_set_id": ["c92335c6-f6fa-4768-9401-55c6b7f87699"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71205-916-00)", "package_ndc": "71205-916-00", "marketing_start_date": "20210708"}], "brand_name": "Penicillamine", "product_id": "71205-916_125ca13e-9784-45be-847a-6fdf9875bd6a", "dosage_form": "CAPSULE", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "71205-916", "generic_name": "Penicillamine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Penicillamine", "active_ingredients": [{"name": "PENICILLAMINE", "strength": "250 mg/1"}], "application_number": "ANDA211735", "marketing_category": "ANDA", "marketing_start_date": "20201221", "listing_expiration_date": "20261231"}