Package 71335-2680-1

Brand: lisinopril

Generic: lisinopril
NDC Package

Package Facts

Identity

Package NDC 71335-2680-1
Digits Only 7133526801
Product NDC 71335-2680
Description

3 TABLET in 1 BOTTLE (71335-2680-1)

Marketing

Marketing Status
Marketed Since 2025-09-12
Brand lisinopril
Generic lisinopril
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d0abda9a-ad4f-4448-9db7-4d1f68b48965", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["314076"], "spl_set_id": ["a0b068b4-1e55-446b-912b-3534e9e6fb75"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET in 1 BOTTLE (71335-2680-1)", "package_ndc": "71335-2680-1", "marketing_start_date": "20250912"}], "brand_name": "LISINOPRIL", "product_id": "71335-2680_d0abda9a-ad4f-4448-9db7-4d1f68b48965", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "71335-2680", "generic_name": "Lisinopril", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LISINOPRIL", "active_ingredients": [{"name": "LISINOPRIL", "strength": "10 mg/1"}], "application_number": "ANDA076164", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}