valsartan

Generic: valsartan

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valsartan
Generic Name valsartan
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

valsartan 160 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6348
Product ID 50090-6348_a4548b54-9d64-45e5-a257-817ffcb85c25
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203311
Listing Expiration 2026-12-31
Marketing Start 2021-06-23

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 500906348
Hyphenated Format 50090-6348

Supplemental Identifiers

RxCUI
349201
UNII
80M03YXJ7I
NUI
N0000000070 N0000175561

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 ANDA203311 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-6348-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-6348-1)
source: ndc

Packages (2)

50090-6348-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-6348-0) 50090-6348-1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6348-1)

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": "a4548b54-9d64-45e5-a257-817ffcb85c25", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["80M03YXJ7I"], "rxcui": ["349201"], "spl_set_id": ["688b5c82-2eba-445c-869e-60609f5db86a"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6348-0)", "package_ndc": "50090-6348-0", "marketing_start_date": "20230126"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6348-1)", "package_ndc": "50090-6348-1", "marketing_start_date": "20230126"}], "brand_name": "Valsartan", "product_id": "50090-6348_a4548b54-9d64-45e5-a257-817ffcb85c25", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-6348", "generic_name": "Valsartan", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan", "active_ingredients": [{"name": "VALSARTAN", "strength": "160 mg/1"}], "application_number": "ANDA203311", "marketing_category": "ANDA", "marketing_start_date": "20210623", "listing_expiration_date": "20261231"}