lisinopril
Generic: lisinopril
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
lisinopril
Generic Name
lisinopril
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
lisinopril 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3409
Product ID
68071-3409_2d6c6950-1dce-5b06-e063-6294a90a779f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077321
Listing Expiration
2026-12-31
Marketing Start
2017-05-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713409
Hyphenated Format
68071-3409
Supplemental Identifiers
RxCUI
UPC
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
lisinopril (source: ndc)
Generic Name
lisinopril (source: ndc)
Application Number
ANDA077321 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 120 TABLET in 1 BOTTLE (68071-3409-2)
- 30 TABLET in 1 BOTTLE (68071-3409-3)
- 90 TABLET in 1 BOTTLE (68071-3409-9)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d6c6950-1dce-5b06-e063-6294a90a779f", "openfda": {"upc": ["0368071340990"], "unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["fbd3bde1-ee64-126f-e053-6394a90a9b6d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (68071-3409-2)", "package_ndc": "68071-3409-2", "marketing_start_date": "20230516"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3409-3)", "package_ndc": "68071-3409-3", "marketing_start_date": "20230516"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3409-9)", "package_ndc": "68071-3409-9", "marketing_start_date": "20230516"}], "brand_name": "Lisinopril", "product_id": "68071-3409_2d6c6950-1dce-5b06-e063-6294a90a779f", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68071-3409", "generic_name": "Lisinopril", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA077321", "marketing_category": "ANDA", "marketing_start_date": "20170512", "listing_expiration_date": "20261231"}