Package 49884-146-01

Brand: penicillamine

Generic: penicillamine
NDC Package

Package Facts

Identity

Package NDC 49884-146-01
Digits Only 4988414601
Product NDC 49884-146
Product ID 49884-146_5c2b4739-a455-4403-ad42-a4e6340064c0
Description

100 CAPSULE in 1 BOTTLE (49884-146-01)

Marketing

Marketing Status
Marketed Since 2020-01-08
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": "5c2b4739-a455-4403-ad42-a4e6340064c0", "openfda": {"nui": ["N0000175713"], "unii": ["GNN1DV99GX"], "rxcui": ["198070"], "spl_set_id": ["01e79d8f-8c74-4f48-b761-9f225fabf93d"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (49884-146-01)", "package_ndc": "49884-146-01", "marketing_start_date": "20200108"}], "brand_name": "Penicillamine", "product_id": "49884-146_5c2b4739-a455-4403-ad42-a4e6340064c0", "dosage_form": "CAPSULE", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "49884-146", "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": "ANDA211231", "marketing_category": "ANDA", "marketing_start_date": "20200108", "listing_expiration_date": "20261231"}