Package 42708-096-30

Brand: lisinopril

Generic: lisinopril
NDC Package Sample

Package Facts

Identity

Package NDC 42708-096-30
Digits Only 4270809630
Product NDC 42708-096
Product ID 42708-096_45b39a1c-a181-f57c-e063-6294a90a8834
Description

30 TABLET in 1 BOTTLE (42708-096-30)

Marketing

Marketing Status
Marketed Since 2018-03-21
Brand lisinopril
Generic lisinopril
Sample Package Yes

Linked Drug Pages (1)

LISINOPRIL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45b39a1c-a181-f57c-e063-6294a90a8834", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["197884"], "spl_set_id": ["cfd31165-5902-4c94-8fff-2940faa983c1"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE (42708-096-30)", "package_ndc": "42708-096-30", "marketing_start_date": "20180321"}], "brand_name": "LISINOPRIL", "product_id": "42708-096_45b39a1c-a181-f57c-e063-6294a90a8834", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "42708-096", "generic_name": "Lisinopril", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LISINOPRIL", "active_ingredients": [{"name": "LISINOPRIL", "strength": "40 mg/1"}], "application_number": "ANDA076164", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}