lisinopril

Generic: lisinopril

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

Drug Facts

Product Profile

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

lisinopril 5 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-176
Product ID 31722-176_cfe12692-404c-ae05-e053-2995a90aa182
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075903
Listing Expiration 2026-12-31
Marketing Start 2021-08-17

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 31722176
Hyphenated Format 31722-176

Supplemental Identifiers

RxCUI
197884 205326 311353 311354 314076 314077
UPC
0331722178013 0331722177016 0331722179010 0331722172011 0331722176019 0331722180016
UNII
E7199S1YWR

Packaging Origin

Original Packager
true

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 ANDA075903 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (31722-176-01)
  • 1000 TABLET in 1 BOTTLE (31722-176-10)
source: ndc

Packages (2)

31722-176-01 100 TABLET in 1 BOTTLE (31722-176-01) 31722-176-10 1000 TABLET in 1 BOTTLE (31722-176-10)

Ingredients (1)

lisinopril (5 mg/1)

Linked Drug Pages (2)

Lisinopril ndc-match (0.9) Lisinopril ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cfe12692-404c-ae05-e053-2995a90aa182", "openfda": {"upc": ["0331722178013", "0331722177016", "0331722179010", "0331722172011", "0331722176019", "0331722180016"], "unii": ["E7199S1YWR"], "rxcui": ["197884", "205326", "311353", "311354", "314076", "314077"], "spl_set_id": ["8f20acd7-2635-4a9b-b732-2a84ea93dea7"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-176-01)", "package_ndc": "31722-176-01", "marketing_start_date": "20210817"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (31722-176-10)", "package_ndc": "31722-176-10", "marketing_start_date": "20210817"}], "brand_name": "Lisinopril", "product_id": "31722-176_cfe12692-404c-ae05-e053-2995a90aa182", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "31722-176", "generic_name": "Lisinopril", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "5 mg/1"}], "application_number": "ANDA075903", "marketing_category": "ANDA", "marketing_start_date": "20210817", "listing_expiration_date": "20261231"}