valsartan

Generic: valsartan

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

Drug Facts

Product Profile

Brand Name valsartan
Generic Name valsartan
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

valsartan 320 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-047
Product ID 62332-047_d9c3b1ac-bbb0-4974-b337-88e247093c72
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091367
Listing Expiration 2026-12-31
Marketing Start 2016-05-20

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 62332047
Hyphenated Format 62332-047

Supplemental Identifiers

RxCUI
349199 349200 349201 349483
UPC
0362332044306 0362332046300
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 ANDA091367 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 320 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (62332-047-30)
  • 500 TABLET in 1 BOTTLE (62332-047-71)
  • 90 TABLET in 1 BOTTLE (62332-047-90)
  • 1000 TABLET in 1 BOTTLE (62332-047-91)
source: ndc

Packages (4)

62332-047-30 30 TABLET in 1 BOTTLE (62332-047-30) 62332-047-71 500 TABLET in 1 BOTTLE (62332-047-71) 62332-047-90 90 TABLET in 1 BOTTLE (62332-047-90) 62332-047-91 1000 TABLET in 1 BOTTLE (62332-047-91)

Ingredients (1)

valsartan (320 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": "d9c3b1ac-bbb0-4974-b337-88e247093c72", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0362332044306", "0362332046300"], "unii": ["80M03YXJ7I"], "rxcui": ["349199", "349200", "349201", "349483"], "spl_set_id": ["8478a05f-38fd-412d-af49-69a73a787c8f"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (62332-047-30)", "package_ndc": "62332-047-30", "marketing_start_date": "20160520"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (62332-047-71)", "package_ndc": "62332-047-71", "marketing_start_date": "20160520"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62332-047-90)", "package_ndc": "62332-047-90", "marketing_start_date": "20160520"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62332-047-91)", "package_ndc": "62332-047-91", "marketing_start_date": "20160520"}], "brand_name": "Valsartan", "product_id": "62332-047_d9c3b1ac-bbb0-4974-b337-88e247093c72", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "62332-047", "generic_name": "Valsartan", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan", "active_ingredients": [{"name": "VALSARTAN", "strength": "320 mg/1"}], "application_number": "ANDA091367", "marketing_category": "ANDA", "marketing_start_date": "20160520", "listing_expiration_date": "20261231"}