valsartan

Generic: valsartan

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valsartan
Generic Name valsartan
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

valsartan 160 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-572
Product ID 65862-572_7b329c09-5c17-4117-9cef-a383ecec90d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202223
Listing Expiration 2026-12-31
Marketing Start 2015-01-05

Pharmacologic Class

Established (EPC)
angiotensin 2 receptor blocker [epc]
Mechanism of Action
angiotensin 2 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862572
Hyphenated Format 65862-572

Supplemental Identifiers

RxCUI
349199 349200 349201 349483
UNII
80M03YXJ7I
NUI
N0000000070 N0000175561

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 valsartan (source: ndc)
Generic Name valsartan (source: ndc)
Application Number ANDA202223 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 CARTON (65862-572-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • 90 TABLET, FILM COATED in 1 BOTTLE (65862-572-90)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (65862-572-99)
source: ndc

Packages (3)

65862-572-10 10 BLISTER PACK in 1 CARTON (65862-572-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK 65862-572-90 90 TABLET, FILM COATED in 1 BOTTLE (65862-572-90) 65862-572-99 1000 TABLET, FILM COATED in 1 BOTTLE (65862-572-99)

Ingredients (1)

valsartan (160 mg/1)

Linked Drug Pages (1)

Valsartan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7b329c09-5c17-4117-9cef-a383ecec90d9", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["80M03YXJ7I"], "rxcui": ["349199", "349200", "349201", "349483"], "spl_set_id": ["a81a72dd-e828-4208-af9b-bb9ac4938537"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-572-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65862-572-10", "marketing_start_date": "20150105"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-572-90)", "package_ndc": "65862-572-90", "marketing_start_date": "20150105"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-572-99)", "package_ndc": "65862-572-99", "marketing_start_date": "20150105"}], "brand_name": "Valsartan", "product_id": "65862-572_7b329c09-5c17-4117-9cef-a383ecec90d9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "65862-572", "generic_name": "Valsartan", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan", "active_ingredients": [{"name": "VALSARTAN", "strength": "160 mg/1"}], "application_number": "ANDA202223", "marketing_category": "ANDA", "marketing_start_date": "20150105", "listing_expiration_date": "20261231"}