olmesartan medoxomil

Generic: olmesartan medoxomil

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

Drug Facts

Product Profile

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

olmesartan medoxomil 20 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-1343
Product ID 70518-1343_48e8efeb-67cd-1cd3-e063-6294a90a2dc1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206763
Listing Expiration 2027-12-31
Marketing Start 2018-08-06

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 705181343
Hyphenated Format 70518-1343

Supplemental Identifiers

RxCUI
349401
UNII
6M97XTV3HD

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 ANDA206763 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1343-0)
source: ndc

Packages (1)

70518-1343-0 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1343-0)

Ingredients (1)

olmesartan medoxomil (20 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": "48e8efeb-67cd-1cd3-e063-6294a90a2dc1", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401"], "spl_set_id": ["92969ed0-8dcd-4c6d-b0c4-e8469c2f65a9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1343-0)", "package_ndc": "70518-1343-0", "marketing_start_date": "20180806"}], "brand_name": "Olmesartan Medoxomil", "product_id": "70518-1343_48e8efeb-67cd-1cd3-e063-6294a90a2dc1", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-1343", "generic_name": "Olmesartan Medoxomil", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA206763", "marketing_category": "ANDA", "marketing_start_date": "20180806", "listing_expiration_date": "20271231"}