lisinopril

Generic: lisinopril

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 10 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4509
Product ID 70518-4509_41aa3a5f-6433-4b28-e063-6294a90ad0c1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076102
Listing Expiration 2026-12-31
Marketing Start 2025-10-20

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184509
Hyphenated Format 70518-4509

Supplemental Identifiers

RxCUI
314076
UNII
E7199S1YWR

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 ANDA076102 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-4509-0)
source: ndc

Packages (1)

70518-4509-0 90 TABLET in 1 BOTTLE, PLASTIC (70518-4509-0)

Ingredients (1)

lisinopril (10 mg/1)

Linked Drug Pages (1)

lisinopril ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41aa3a5f-6433-4b28-e063-6294a90ad0c1", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["314076"], "spl_set_id": ["c57e8bc8-ff50-431e-9c1a-384503584d02"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4509-0)", "package_ndc": "70518-4509-0", "marketing_start_date": "20251020"}], "brand_name": "lisinopril", "product_id": "70518-4509_41aa3a5f-6433-4b28-e063-6294a90ad0c1", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "70518-4509", "generic_name": "lisinopril", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "10 mg/1"}], "application_number": "ANDA076102", "marketing_category": "ANDA", "marketing_start_date": "20251020", "listing_expiration_date": "20261231"}