olmesartan medoxomil and hydrochlorothiazide
Generic: olmesartan medoxomil and hydrochlorothiazide
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
olmesartan medoxomil and hydrochlorothiazide
Generic Name
olmesartan medoxomil and hydrochlorothiazide
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
hydrochlorothiazide 25 mg/1, olmesartan medoxomil 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-4307
Product ID
63629-4307_4260e974-b777-48b2-9ec2-af8e91e2ef6c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204233
Listing Expiration
2026-12-31
Marketing Start
2017-04-24
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636294307
Hyphenated Format
63629-4307
Supplemental Identifiers
RxCUI
UNII
NUI
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 and hydrochlorothiazide (source: ndc)
Generic Name
olmesartan medoxomil and hydrochlorothiazide (source: ndc)
Application Number
ANDA204233 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
- 40 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (63629-4307-1)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4260e974-b777-48b2-9ec2-af8e91e2ef6c", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403855"], "spl_set_id": ["e8a9dcaa-04e3-4f4e-a53d-42903e3da2d4"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-4307-1)", "package_ndc": "63629-4307-1", "marketing_start_date": "20240626"}], "brand_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "product_id": "63629-4307_4260e974-b777-48b2-9ec2-af8e91e2ef6c", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "63629-4307", "generic_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA204233", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}