valsartan

Generic: valsartan

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

Drug Facts

Product Profile

Brand Name valsartan
Generic Name valsartan
Labeler ohm laboratories inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

valsartan 320 mg/1

Manufacturer
Ohm Laboratories Inc.

Identifiers & Regulatory

Product NDC 51660-143
Product ID 51660-143_0ea6cbb4-10cd-fecf-e063-6394a90a513b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077492
Listing Expiration 2026-12-31
Marketing Start 2014-07-07

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 51660143
Hyphenated Format 51660-143

Supplemental Identifiers

RxCUI
349199 349200 349201 349483
UPC
0351660140309
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 ANDA077492 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 320 mg/1
source: ndc
Packaging
  • 10 TABLET, FILM COATED in 1 BOTTLE (51660-143-03)
  • 500 TABLET, FILM COATED in 1 BOTTLE (51660-143-05)
  • 90 TABLET, FILM COATED in 1 BOTTLE (51660-143-90)
source: ndc

Packages (3)

51660-143-03 10 TABLET, FILM COATED in 1 BOTTLE (51660-143-03) 51660-143-05 500 TABLET, FILM COATED in 1 BOTTLE (51660-143-05) 51660-143-90 90 TABLET, FILM COATED in 1 BOTTLE (51660-143-90)

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": "0ea6cbb4-10cd-fecf-e063-6394a90a513b", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0351660140309"], "unii": ["80M03YXJ7I"], "rxcui": ["349199", "349200", "349201", "349483"], "spl_set_id": ["ab5e0e5a-5bdf-4cfc-9d18-57ea4d642f65"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Ohm Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (51660-143-03)", "package_ndc": "51660-143-03", "marketing_start_date": "20140707"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (51660-143-05)", "package_ndc": "51660-143-05", "marketing_start_date": "20140707"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (51660-143-90)", "package_ndc": "51660-143-90", "marketing_start_date": "20140707"}], "brand_name": "VALSARTAN", "product_id": "51660-143_0ea6cbb4-10cd-fecf-e063-6394a90a513b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "51660-143", "generic_name": "VALSARTAN", "labeler_name": "Ohm Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VALSARTAN", "active_ingredients": [{"name": "VALSARTAN", "strength": "320 mg/1"}], "application_number": "ANDA077492", "marketing_category": "ANDA", "marketing_start_date": "20140707", "listing_expiration_date": "20261231"}