lisinopril

Generic: lisinopril

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

lisinopril 40 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-815
Product ID 43063-815_415b9940-77ea-a174-e063-6294a90a4cfe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075743
Listing Expiration 2026-12-31
Marketing Start 2017-08-30

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 43063815
Hyphenated Format 43063-815

Supplemental Identifiers

RxCUI
197884 205326 311353 311354 314076 314077
UPC
0343063810019 0343063814017 0343063813010 0343063812013
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 ANDA075743 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (43063-815-01)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-815-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-815-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-815-90)
source: ndc

Packages (4)

43063-815-01 100 TABLET in 1 BOTTLE, PLASTIC (43063-815-01) 43063-815-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-815-30) 43063-815-60 60 TABLET in 1 BOTTLE, PLASTIC (43063-815-60) 43063-815-90 90 TABLET in 1 BOTTLE, PLASTIC (43063-815-90)

Ingredients (1)

lisinopril (40 mg/1)

Linked Drug Pages (1)

Lisinopril ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "415b9940-77ea-a174-e063-6294a90a4cfe", "openfda": {"upc": ["0343063810019", "0343063814017", "0343063813010", "0343063812013"], "unii": ["E7199S1YWR"], "rxcui": ["197884", "205326", "311353", "311354", "314076", "314077"], "spl_set_id": ["b62815f3-77fc-4074-a28a-918ab5cc32db"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (43063-815-01)", "package_ndc": "43063-815-01", "marketing_start_date": "20180105"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-815-30)", "package_ndc": "43063-815-30", "marketing_start_date": "20180108"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-815-60)", "package_ndc": "43063-815-60", "marketing_start_date": "20180111"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-815-90)", "package_ndc": "43063-815-90", "marketing_start_date": "20180109"}], "brand_name": "Lisinopril", "product_id": "43063-815_415b9940-77ea-a174-e063-6294a90a4cfe", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "43063-815", "generic_name": "Lisinopril", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "40 mg/1"}], "application_number": "ANDA075743", "marketing_category": "ANDA", "marketing_start_date": "20170830", "listing_expiration_date": "20261231"}