Package 70748-153-01

Brand: penicillamine

Generic: penicillamine
NDC Package

Package Facts

Identity

Package NDC 70748-153-01
Digits Only 7074815301
Product NDC 70748-153
Product ID 70748-153_99f3ca78-1663-47a1-9ed3-9c4eaa9f0271
Description

100 TABLET in 1 BOTTLE (70748-153-01)

Marketing

Marketing Status
Marketed Since 2021-03-01
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": "99f3ca78-1663-47a1-9ed3-9c4eaa9f0271", "openfda": {"nui": ["N0000175713"], "upc": ["0370748153017"], "unii": ["GNN1DV99GX"], "rxcui": ["198071"], "spl_set_id": ["f6ecaf47-902f-4378-b524-7a88f20ba138"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70748-153-01)", "package_ndc": "70748-153-01", "marketing_start_date": "20210301"}], "brand_name": "Penicillamine", "product_id": "70748-153_99f3ca78-1663-47a1-9ed3-9c4eaa9f0271", "dosage_form": "TABLET", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "70748-153", "generic_name": "Penicillamine", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Penicillamine", "active_ingredients": [{"name": "PENICILLAMINE", "strength": "250 mg/1"}], "application_number": "ANDA212933", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}