lisinopril

Generic: lisinopril

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 5 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3123
Product ID 68071-3123_1d9eaa76-8491-a471-e063-6394a90aef30
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076180
Listing Expiration 2026-12-31
Marketing Start 2011-11-01

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713123
Hyphenated Format 68071-3123

Supplemental Identifiers

RxCUI
311354
UPC
0368071312331
UNII
E7199S1YWR

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 ANDA076180 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 120 TABLET in 1 BOTTLE (68071-3123-1)
  • 30 TABLET in 1 BOTTLE (68071-3123-3)
  • 60 TABLET in 1 BOTTLE (68071-3123-6)
  • 90 TABLET in 1 BOTTLE (68071-3123-9)
source: ndc

Packages (4)

Ingredients (1)

lisinopril (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d9eaa76-8491-a471-e063-6394a90aef30", "openfda": {"upc": ["0368071312331"], "unii": ["E7199S1YWR"], "rxcui": ["311354"], "spl_set_id": ["4aa44af9-1aff-314c-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (68071-3123-1)", "package_ndc": "68071-3123-1", "marketing_start_date": "20170313"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3123-3)", "package_ndc": "68071-3123-3", "marketing_start_date": "20170313"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3123-6)", "package_ndc": "68071-3123-6", "marketing_start_date": "20170313"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3123-9)", "package_ndc": "68071-3123-9", "marketing_start_date": "20170313"}], "brand_name": "LISINOPRIL", "product_id": "68071-3123_1d9eaa76-8491-a471-e063-6394a90aef30", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68071-3123", "generic_name": "Lisinopril", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LISINOPRIL", "active_ingredients": [{"name": "LISINOPRIL", "strength": "5 mg/1"}], "application_number": "ANDA076180", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}