olmesartan medoxomil

Generic: olmesartan medoxomil

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

Drug Facts

Product Profile

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

olmesartan medoxomil 5 mg/1

Manufacturer
Alembic Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 46708-131
Product ID 46708-131_03dfb859-492b-4154-8fc7-dc4fa90cbf59
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 46708131
Hyphenated Format 46708-131

Supplemental Identifiers

RxCUI
349373 349401 349405
UPC
0346708132309 0346708133306 0346708131302
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 (46708-131-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (46708-131-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (46708-131-90)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (46708-131-91)
source: ndc

Packages (4)

46708-131-10 100 TABLET, FILM COATED in 1 CARTON (46708-131-10) 46708-131-30 30 TABLET, FILM COATED in 1 BOTTLE (46708-131-30) 46708-131-90 90 TABLET, FILM COATED in 1 BOTTLE (46708-131-90) 46708-131-91 1000 TABLET, FILM COATED in 1 BOTTLE (46708-131-91)

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": "03dfb859-492b-4154-8fc7-dc4fa90cbf59", "openfda": {"upc": ["0346708132309", "0346708133306", "0346708131302"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["ac08ea7d-f529-42ca-850a-a0ecce7dc830"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 CARTON (46708-131-10)", "package_ndc": "46708-131-10", "marketing_start_date": "20170424"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (46708-131-30)", "package_ndc": "46708-131-30", "marketing_start_date": "20170424"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (46708-131-90)", "package_ndc": "46708-131-90", "marketing_start_date": "20170424"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-131-91)", "package_ndc": "46708-131-91", "marketing_start_date": "20170424"}], "brand_name": "Olmesartan Medoxomil", "product_id": "46708-131_03dfb859-492b-4154-8fc7-dc4fa90cbf59", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "46708-131", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Alembic Pharmaceuticals Limited", "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"}