Package 42708-154-30

Brand: lisinopril

Generic: lisinopril
NDC Package Sample

Package Facts

Identity

Package NDC 42708-154-30
Digits Only 4270815430
Product NDC 42708-154
Description

30 TABLET in 1 BOTTLE (42708-154-30)

Marketing

Marketing Status
Marketed Since 2022-08-04
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": "4681c975-bd22-3231-e063-6394a90a969f", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["314076"], "spl_set_id": ["e56f3738-3103-3ba4-e053-2a95a90aebb4"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE (42708-154-30)", "package_ndc": "42708-154-30", "marketing_start_date": "20220804"}], "brand_name": "Lisinopril", "product_id": "42708-154_4681c975-bd22-3231-e063-6394a90a969f", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "42708-154", "generic_name": "Lisinopril", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "10 mg/1"}], "application_number": "ANDA077321", "marketing_category": "ANDA", "marketing_start_date": "20170512", "listing_expiration_date": "20261231"}