lisinopril

Generic: lisinopril

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler bluepoint laboratories
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 20 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-335
Product ID 68001-335_c5fac2c4-de1f-49d3-e053-2a95a90a5285
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077321
Listing Expiration 2026-12-31
Marketing Start 2017-08-01

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 68001335
Hyphenated Format 68001-335

Supplemental Identifiers

RxCUI
197884 205326 311353 311354 314076 314077
UPC
0368001334082
UNII
E7199S1YWR

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68001-335-00)
  • 1000 TABLET in 1 BOTTLE (68001-335-08)
source: ndc

Packages (2)

68001-335-00 100 TABLET in 1 BOTTLE (68001-335-00) 68001-335-08 1000 TABLET in 1 BOTTLE (68001-335-08)

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": "c5fac2c4-de1f-49d3-e053-2a95a90a5285", "openfda": {"upc": ["0368001334082"], "unii": ["E7199S1YWR"], "rxcui": ["197884", "205326", "311353", "311354", "314076", "314077"], "spl_set_id": ["34ebeea1-6812-4697-84c4-b2ae4f39e55f"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68001-335-00)", "package_ndc": "68001-335-00", "marketing_start_date": "20170801"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68001-335-08)", "package_ndc": "68001-335-08", "marketing_start_date": "20170801"}], "brand_name": "Lisinopril", "product_id": "68001-335_c5fac2c4-de1f-49d3-e053-2a95a90a5285", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68001-335", "generic_name": "Lisinopril", "labeler_name": "BluePoint Laboratories", "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": "20170801", "listing_expiration_date": "20261231"}