moexipril hydrochloride

Generic: moexipril hydrochloride

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

Drug Facts

Product Profile

Brand Name moexipril hydrochloride
Generic Name moexipril hydrochloride
Labeler chartwell rx, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

moexipril hydrochloride 15 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-969
Product ID 62135-969_3001c14d-1545-86fb-e063-6294a90a035f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077536
Listing Expiration 2026-12-31
Marketing Start 2006-11-30

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 62135969
Hyphenated Format 62135-969

Supplemental Identifiers

RxCUI
1299896 1299897
UPC
0362135967901 0362135969905
UNII
Q1UMG3UH45

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 moexipril hydrochloride (source: ndc)
Generic Name moexipril hydrochloride (source: ndc)
Application Number ANDA077536 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (62135-969-90)
source: ndc

Packages (1)

62135-969-90 90 TABLET, FILM COATED in 1 BOTTLE (62135-969-90)

Ingredients (1)

moexipril hydrochloride (15 mg/1)

Linked Drug Pages (1)

Moexipril Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3001c14d-1545-86fb-e063-6294a90a035f", "openfda": {"upc": ["0362135967901", "0362135969905"], "unii": ["Q1UMG3UH45"], "rxcui": ["1299896", "1299897"], "spl_set_id": ["5c24072c-9769-4cb5-b8da-bf814d21391d"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-969-90)", "package_ndc": "62135-969-90", "marketing_start_date": "20250305"}], "brand_name": "Moexipril Hydrochloride", "product_id": "62135-969_3001c14d-1545-86fb-e063-6294a90a035f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "62135-969", "generic_name": "Moexipril Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moexipril Hydrochloride", "active_ingredients": [{"name": "MOEXIPRIL HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA077536", "marketing_category": "ANDA", "marketing_start_date": "20061130", "listing_expiration_date": "20261231"}