olmesartan medoxomil

Generic: olmesartan medoxomil

Labeler: alembic pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name olmesartan medoxomil
Generic Name olmesartan medoxomil
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

olmesartan medoxomil 5 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-131
Product ID 62332-131_95e8d157-e834-4d1d-9520-8ee05f8ca69b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203012
Listing Expiration 2026-12-31
Marketing Start 2017-04-24

Pharmacologic Class

Classes
angiotensin 2 receptor antagonists [moa] angiotensin 2 receptor blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62332131
Hyphenated Format 62332-131

Supplemental Identifiers

RxCUI
349373 349401 349405
UPC
0362332133307 0362332132300 0362332131303
UNII
6M97XTV3HD

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 olmesartan medoxomil (source: ndc)
Generic Name olmesartan medoxomil (source: ndc)
Application Number ANDA203012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 CARTON (62332-131-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (62332-131-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (62332-131-90)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (62332-131-91)
source: ndc

Packages (4)

62332-131-10 100 TABLET, FILM COATED in 1 CARTON (62332-131-10) 62332-131-30 30 TABLET, FILM COATED in 1 BOTTLE (62332-131-30) 62332-131-90 90 TABLET, FILM COATED in 1 BOTTLE (62332-131-90) 62332-131-91 1000 TABLET, FILM COATED in 1 BOTTLE (62332-131-91)

Ingredients (1)

olmesartan medoxomil (5 mg/1)

Linked Drug Pages (1)

Olmesartan Medoxomil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "95e8d157-e834-4d1d-9520-8ee05f8ca69b", "openfda": {"upc": ["0362332133307", "0362332132300", "0362332131303"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["cf4f62f9-5a00-4313-b703-ec0ac6380b5e"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 CARTON (62332-131-10)", "package_ndc": "62332-131-10", "marketing_start_date": "20170424"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-131-30)", "package_ndc": "62332-131-30", "marketing_start_date": "20170424"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62332-131-90)", "package_ndc": "62332-131-90", "marketing_start_date": "20170424"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-131-91)", "package_ndc": "62332-131-91", "marketing_start_date": "20170424"}], "brand_name": "Olmesartan Medoxomil", "product_id": "62332-131_95e8d157-e834-4d1d-9520-8ee05f8ca69b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "62332-131", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "5 mg/1"}], "application_number": "ANDA203012", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}