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 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-800
Product ID
43063-800_3284fe75-4071-2f1a-e063-6294a90ac895
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076164
Listing Expiration
2026-12-31
Marketing Start
2011-11-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063800
Hyphenated Format
43063-800
Supplemental Identifiers
RxCUI
UPC
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
ANDA076164 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-800-30)
- 90 TABLET in 1 BOTTLE, PLASTIC (43063-800-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3284fe75-4071-2f1a-e063-6294a90ac895", "openfda": {"upc": ["0343063800300"], "unii": ["E7199S1YWR"], "rxcui": ["197884"], "spl_set_id": ["dd015c18-1ea6-44e3-9186-8d2f8444d874"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-800-30)", "package_ndc": "43063-800-30", "marketing_start_date": "20171025"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-800-90)", "package_ndc": "43063-800-90", "marketing_start_date": "20171027"}], "brand_name": "LISINOPRIL", "product_id": "43063-800_3284fe75-4071-2f1a-e063-6294a90ac895", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "43063-800", "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": "ANDA076164", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}