lisinopril
Generic: lisinopril
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
lisinopril
Generic Name
lisinopril
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
lisinopril 20 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789093
Hyphenated Format
72789-093
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (72789-093-30)
- 90 TABLET in 1 BOTTLE, PLASTIC (72789-093-90)
Packages (2)
Ingredients (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"}