moexipril hydrochloride

Generic: moexipril hydrochloride

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name moexipril hydrochloride
Generic Name moexipril hydrochloride
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

moexipril hydrochloride 7.5 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-0017
Product ID 0093-0017_2c29e2eb-8956-4fb2-a371-57466c82f348
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076204
Listing Expiration 2026-12-31
Marketing Start 2003-05-08

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 00930017
Hyphenated Format 0093-0017

Supplemental Identifiers

RxCUI
1299896 1299897
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 ANDA076204 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0093-0017-01)
source: ndc

Packages (1)

0093-0017-01 100 TABLET, FILM COATED in 1 BOTTLE (0093-0017-01)

Ingredients (1)

moexipril hydrochloride (7.5 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": "2c29e2eb-8956-4fb2-a371-57466c82f348", "openfda": {"unii": ["Q1UMG3UH45"], "rxcui": ["1299896", "1299897"], "spl_set_id": ["5d4078f3-b621-475f-a4e6-005de2e62b32"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-0017-01)", "package_ndc": "0093-0017-01", "marketing_start_date": "20030508"}], "brand_name": "Moexipril Hydrochloride", "product_id": "0093-0017_2c29e2eb-8956-4fb2-a371-57466c82f348", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "0093-0017", "generic_name": "Moexipril Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moexipril Hydrochloride", "active_ingredients": [{"name": "MOEXIPRIL HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA076204", "marketing_category": "ANDA", "marketing_start_date": "20030508", "listing_expiration_date": "20261231"}