lisinopril

Generic: lisinopril

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 10 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-642
Product ID 62135-642_462a5023-e5a0-692a-e063-6294a90a7236
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212041
Listing Expiration 2026-12-31
Marketing Start 2020-09-15

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 62135642
Hyphenated Format 62135-642

Supplemental Identifiers

RxCUI
197884 205326 311353 311354 314076 314077
UPC
0362135641313 0362135643317 0362135641900 0362135645311 0362135643904 0362135642907 0362135640316 0362135644901 0362135645908 0362135644314 0362135640903 0362135642310
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 ANDA212041 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 300 TABLET in 1 BOTTLE (62135-642-31)
  • 90 TABLET in 1 BOTTLE (62135-642-90)
source: ndc

Packages (2)

Ingredients (1)

lisinopril (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "462a5023-e5a0-692a-e063-6294a90a7236", "openfda": {"upc": ["0362135641313", "0362135643317", "0362135641900", "0362135645311", "0362135643904", "0362135642907", "0362135640316", "0362135644901", "0362135645908", "0362135644314", "0362135640903", "0362135642310"], "unii": ["E7199S1YWR"], "rxcui": ["197884", "205326", "311353", "311354", "314076", "314077"], "spl_set_id": ["8824e5e5-ed35-4a95-bfd6-98a2e7c4bbce"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (62135-642-31)", "package_ndc": "62135-642-31", "marketing_start_date": "20230607"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-642-90)", "package_ndc": "62135-642-90", "marketing_start_date": "20230607"}], "brand_name": "Lisinopril", "product_id": "62135-642_462a5023-e5a0-692a-e063-6294a90a7236", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "62135-642", "generic_name": "Lisinopril", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "10 mg/1"}], "application_number": "ANDA212041", "marketing_category": "ANDA", "marketing_start_date": "20200915", "listing_expiration_date": "20261231"}