lisinopril
Generic: lisinopril
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
lisinopril
Generic Name
lisinopril
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
lisinopril 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-1156
Product ID
70518-1156_48bf7dc4-10cb-49f1-e063-6394a90a03d8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077321
Listing Expiration
2027-12-31
Marketing Start
2018-05-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705181156
Hyphenated Format
70518-1156
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 BLISTER PACK (70518-1156-0)
- 60 TABLET in 1 BLISTER PACK (70518-1156-2)
- 30 TABLET in 1 BOTTLE, PLASTIC (70518-1156-4)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48bf7dc4-10cb-49f1-e063-6394a90a03d8", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["3451292b-7867-4dc2-afaa-da66b4016017"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1156-0)", "package_ndc": "70518-1156-0", "marketing_start_date": "20180502"}, {"sample": false, "description": "60 TABLET in 1 BLISTER PACK (70518-1156-2)", "package_ndc": "70518-1156-2", "marketing_start_date": "20210719"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-1156-4)", "package_ndc": "70518-1156-4", "marketing_start_date": "20250521"}], "brand_name": "Lisinopril", "product_id": "70518-1156_48bf7dc4-10cb-49f1-e063-6394a90a03d8", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "70518-1156", "generic_name": "Lisinopril", "labeler_name": "REMEDYREPACK 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": "20180502", "listing_expiration_date": "20271231"}