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 20 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-5098
Product ID 68071-5098_2cc859a5-f9c7-8eae-e063-6294a90ab4b5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076059
Listing Expiration 2026-12-31
Marketing Start 2002-07-01

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 680715098
Hyphenated Format 68071-5098

Supplemental Identifiers

RxCUI
314077
UPC
0368071509892
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 ANDA076059 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (68071-5098-9)
source: ndc

Packages (1)

Ingredients (1)

lisinopril (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2cc859a5-f9c7-8eae-e063-6294a90ab4b5", "openfda": {"upc": ["0368071509892"], "unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["964c7f28-f62e-30b5-e053-2a95a90ab84c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-5098-9)", "package_ndc": "68071-5098-9", "marketing_start_date": "20191101"}], "brand_name": "Lisinopril", "product_id": "68071-5098_2cc859a5-f9c7-8eae-e063-6294a90ab4b5", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68071-5098", "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": "ANDA076059", "marketing_category": "ANDA", "marketing_start_date": "20020701", "listing_expiration_date": "20261231"}