Package 42708-032-30
Brand: lisinopril
Generic: lisinoprilPackage 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
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"}