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 2.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-1316
Product ID
70518-1316_48d5a523-2a72-7609-e063-6394a90a4e2e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077321
Listing Expiration
2027-12-31
Marketing Start
2018-07-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705181316
Hyphenated Format
70518-1316
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
- 2.5 mg/1
Packaging
- 30 TABLET in 1 BLISTER PACK (70518-1316-0)
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-1316-1)
- 100 TABLET in 1 BOTTLE, PLASTIC (70518-1316-4)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48d5a523-2a72-7609-e063-6394a90a4e2e", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["311353"], "spl_set_id": ["d32923fe-a323-43c6-af46-bcba7274b0bf"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1316-0)", "package_ndc": "70518-1316-0", "marketing_start_date": "20180723"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-1316-1)", "package_ndc": "70518-1316-1", "marketing_start_date": "20200203"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-1316-4)", "package_ndc": "70518-1316-4", "marketing_start_date": "20250321"}], "brand_name": "Lisinopril", "product_id": "70518-1316_48d5a523-2a72-7609-e063-6394a90a4e2e", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "70518-1316", "generic_name": "Lisinopril", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "2.5 mg/1"}], "application_number": "ANDA077321", "marketing_category": "ANDA", "marketing_start_date": "20180723", "listing_expiration_date": "20271231"}