Package 42708-142-30

Brand: lisinopril

Generic: lisinopril
NDC Package Sample

Package Facts

Identity

Package NDC 42708-142-30
Digits Only 4270814230
Product NDC 42708-142
Description

30 TABLET in 1 BOTTLE (42708-142-30)

Marketing

Marketing Status
Marketed Since 2021-03-10
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": "459bebab-b18e-58b4-e063-6294a90ad140", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["bd436b8b-98a6-584c-e053-2995a90ac15d"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE (42708-142-30)", "package_ndc": "42708-142-30", "marketing_start_date": "20210310"}], "brand_name": "LISINOPRIL", "product_id": "42708-142_459bebab-b18e-58b4-e063-6294a90ad140", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "42708-142", "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": "ANDA076164", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}