lisinopril

Generic: lisinopril

Labeler: redpharm drug, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler redpharm drug, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 20 mg/1

Manufacturer
RedPharm Drug, Inc.

Identifiers & Regulatory

Product NDC 67296-1202
Product ID 67296-1202_490debf7-a097-8582-e063-6394a90a851e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076164
Listing Expiration 2027-12-31
Marketing Start 2011-11-01

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 672961202
Hyphenated Format 67296-1202

Supplemental Identifiers

RxCUI
314077
UPC
0367296120295
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 BOTTLE (67296-1202-3)
  • 90 TABLET in 1 BOTTLE (67296-1202-9)
source: ndc

Packages (2)

67296-1202-3 30 TABLET in 1 BOTTLE (67296-1202-3) 67296-1202-9 90 TABLET in 1 BOTTLE (67296-1202-9)

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": "490debf7-a097-8582-e063-6394a90a851e", "openfda": {"upc": ["0367296120295"], "unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["4f08cfc9-7afc-33aa-e054-00144ff88e88"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-1202-3)", "package_ndc": "67296-1202-3", "marketing_start_date": "20111101"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (67296-1202-9)", "package_ndc": "67296-1202-9", "marketing_start_date": "20111101"}], "brand_name": "LISINOPRIL", "product_id": "67296-1202_490debf7-a097-8582-e063-6394a90a851e", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "67296-1202", "generic_name": "LISINOPRIL", "labeler_name": "RedPharm Drug, 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": "20111101", "listing_expiration_date": "20271231"}