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 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55289-884
Product ID
55289-884_2ac07d8b-fa54-8926-e063-6294a90a0e06
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077321
Listing Expiration
2026-12-31
Marketing Start
2006-01-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55289884
Hyphenated Format
55289-884
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
ANDA077321 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (55289-884-30)
- 90 TABLET in 1 BOTTLE, PLASTIC (55289-884-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2ac07d8b-fa54-8926-e063-6294a90a0e06", "openfda": {"upc": ["0355289884309"], "unii": ["E7199S1YWR"], "rxcui": ["311354"], "spl_set_id": ["c621c33b-cb67-4ea6-b2bd-96c20a244ea4"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (55289-884-30)", "package_ndc": "55289-884-30", "marketing_start_date": "20110408"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (55289-884-90)", "package_ndc": "55289-884-90", "marketing_start_date": "20110408"}], "brand_name": "Lisinopril", "product_id": "55289-884_2ac07d8b-fa54-8926-e063-6294a90a0e06", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "55289-884", "generic_name": "Lisinopril", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "5 mg/1"}], "application_number": "ANDA077321", "marketing_category": "ANDA", "marketing_start_date": "20060113", "listing_expiration_date": "20261231"}