valsartan

Generic: valsartan

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valsartan
Generic Name valsartan
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

valsartan 320 mg/1

Manufacturer
Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-235
Product ID 29300-235_4d1e743f-8954-4634-b95b-adb7ae41a549
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209261
Listing Expiration 2026-12-31
Marketing Start 2018-05-04

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 29300235
Hyphenated Format 29300-235

Supplemental Identifiers

RxCUI
349199 349200 349201 349483
UPC
0329300233193 0329300232196 0329300234190 0329300235197
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 ANDA209261 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 320 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-13)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-19)
source: ndc

Packages (3)

29300-235-10 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-10) 29300-235-13 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-13) 29300-235-19 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-19)

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": "4d1e743f-8954-4634-b95b-adb7ae41a549", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0329300233193", "0329300232196", "0329300234190", "0329300235197"], "unii": ["80M03YXJ7I"], "rxcui": ["349199", "349200", "349201", "349483"], "spl_set_id": ["93b82a9f-dc0a-4f7d-b0d4-4adf0d917b7e"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-10)", "package_ndc": "29300-235-10", "marketing_start_date": "20180515"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-13)", "package_ndc": "29300-235-13", "marketing_start_date": "20180515"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-235-19)", "package_ndc": "29300-235-19", "marketing_start_date": "20180515"}], "brand_name": "Valsartan", "product_id": "29300-235_4d1e743f-8954-4634-b95b-adb7ae41a549", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "29300-235", "generic_name": "Valsartan", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan", "active_ingredients": [{"name": "VALSARTAN", "strength": "320 mg/1"}], "application_number": "ANDA209261", "marketing_category": "ANDA", "marketing_start_date": "20180504", "listing_expiration_date": "20261231"}