Package 42708-032-30

Brand: lisinopril

Generic: lisinopril
NDC Package Sample

Package Facts

Identity

Package NDC 42708-032-30
Digits Only 4270803230
Product NDC 42708-032
Description

30 TABLET in 1 BOTTLE, PLASTIC (42708-032-30)

Marketing

Marketing Status
Marketed Since 2018-03-14
Brand lisinopril
Generic lisinopril
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45b3fff5-b53d-af7e-e063-6394a90aeeea", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["197884", "314076", "314077"], "spl_set_id": ["b17cd16b-8d0a-4cfa-bd48-2529983fcd12"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE, PLASTIC (42708-032-30)", "package_ndc": "42708-032-30", "marketing_start_date": "20180314"}], "brand_name": "Lisinopril", "product_id": "42708-032_45b3fff5-b53d-af7e-e063-6394a90aeeea", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "42708-032", "generic_name": "Lisinopril", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA076059", "marketing_category": "ANDA", "marketing_start_date": "20020701", "listing_expiration_date": "20261231"}