valsartan and hydrochlorothiazide
Generic: valsartan and hydrochlorothiazide
Labeler: solco healthcare us, llcDrug Facts
Product Profile
Brand Name
valsartan and hydrochlorothiazide
Generic Name
valsartan and hydrochlorothiazide
Labeler
solco healthcare us, llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
hydrochlorothiazide 12.5 mg/1, valsartan 80 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43547-311
Product ID
43547-311_1b876e29-1212-4e28-8d3c-e2e717a8fe53
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206083
Listing Expiration
2026-12-31
Marketing Start
2015-10-31
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43547311
Hyphenated Format
43547-311
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
valsartan and hydrochlorothiazide (source: ndc)
Generic Name
valsartan and hydrochlorothiazide (source: ndc)
Application Number
ANDA206083 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12.5 mg/1
- 80 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (43547-311-03)
- 90 TABLET, FILM COATED in 1 BOTTLE (43547-311-09)
- 500 TABLET, FILM COATED in 1 BOTTLE (43547-311-50)
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b876e29-1212-4e28-8d3c-e2e717a8fe53", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "upc": ["0343547313036", "0343547314033", "0343547315030", "0343547311032", "0343547312039"], "unii": ["0J48LPH2TH", "80M03YXJ7I"], "rxcui": ["200284", "200285", "349353", "636042", "636045"], "spl_set_id": ["f8b0a8ab-4549-4553-a127-bf2c0291a4b1"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Solco Healthcare US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (43547-311-03)", "package_ndc": "43547-311-03", "marketing_start_date": "20211203"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (43547-311-09)", "package_ndc": "43547-311-09", "marketing_start_date": "20211203"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (43547-311-50)", "package_ndc": "43547-311-50", "marketing_start_date": "20211203"}], "brand_name": "VALSARTAN AND HYDROCHLOROTHIAZIDE", "product_id": "43547-311_1b876e29-1212-4e28-8d3c-e2e717a8fe53", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "43547-311", "generic_name": "valsartan and hydrochlorothiazide", "labeler_name": "Solco Healthcare US, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VALSARTAN AND HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "VALSARTAN", "strength": "80 mg/1"}], "application_number": "ANDA206083", "marketing_category": "ANDA", "marketing_start_date": "20151031", "listing_expiration_date": "20261231"}