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 20 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-0845
Product ID 70518-0845_4845821f-fc64-be02-e063-6394a90aeb42
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076164
Listing Expiration 2027-12-31
Marketing Start 2017-11-13

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 705180845
Hyphenated Format 70518-0845

Supplemental Identifiers

RxCUI
314077
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 ANDA076164 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-0845-2)
source: ndc

Packages (1)

70518-0845-2 30 TABLET in 1 BLISTER PACK (70518-0845-2)

Ingredients (1)

lisinopril (20 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": "4845821f-fc64-be02-e063-6394a90aeb42", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["e17bcc2e-f5ed-4846-95d3-a5479c7fee8d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0845-2)", "package_ndc": "70518-0845-2", "marketing_start_date": "20251029"}], "brand_name": "LISINOPRIL", "product_id": "70518-0845_4845821f-fc64-be02-e063-6394a90aeb42", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "70518-0845", "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": "ANDA076164", "marketing_category": "ANDA", "marketing_start_date": "20171113", "listing_expiration_date": "20271231"}