NDC 71335-0600

Valsartan

Valsartan

Valsartan is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Valsartan.

Product ID71335-0600_3d3425ce-596a-483e-82e9-24a9e6d09f50
NDC71335-0600
Product TypeHuman Prescription Drug
Proprietary NameValsartan
Generic NameValsartan
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2015-01-05
Marketing CategoryANDA / ANDA
Application NumberANDA090642
Labeler NameBryant Ranch Prepack
Substance NameVALSARTAN
Active Ingredient Strength320 mg/1
Pharm ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71335-0600-2

90 TABLET, FILM COATED in 1 BOTTLE (71335-0600-2)
Marketing Start Date2017-11-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0600-3 [71335060003]

Valsartan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090642
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-11-22
Marketing End Date2017-12-31

NDC 71335-0600-1 [71335060001]

Valsartan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090642
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-11-22
Marketing End Date2017-12-31

NDC 71335-0600-2 [71335060002]

Valsartan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090642
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-11-22
Marketing End Date2017-12-31

Drug Details

Active Ingredients

IngredientStrength
VALSARTAN320 mg/1

OpenFDA Data

SPL SET ID:5badb230-b08a-4b2d-a15c-0593cad8b8a7
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 349200
  • 349201

    • Pharmacological Class

    • Angiotensin 2 Receptor Antagonists [MoA]
    • Angiotensin 2 Receptor Blocker [EPC]