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 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-093
Product ID 72789-093_3ca56f64-b651-2dca-e063-6294a90aec70
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077321
Listing Expiration 2026-12-31
Marketing Start 2017-05-12

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 72789093
Hyphenated Format 72789-093

Supplemental Identifiers

RxCUI
314077
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 ANDA077321 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-093-30)
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-093-90)
source: ndc

Packages (2)

Ingredients (1)

lisinopril (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ca56f64-b651-2dca-e063-6294a90aec70", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["9470b102-3c81-469a-a4c5-6816d9d39b07"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-093-30)", "package_ndc": "72789-093-30", "marketing_start_date": "20200623"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-093-90)", "package_ndc": "72789-093-90", "marketing_start_date": "20200619"}], "brand_name": "Lisinopril", "product_id": "72789-093_3ca56f64-b651-2dca-e063-6294a90aec70", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "72789-093", "generic_name": "Lisinopril", "labeler_name": "PD-Rx 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"}