NDC 68788-6882

Valsartan

Valsartan

Valsartan is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Valsartan.

Product ID68788-6882_fe3a18ca-1f3a-40d2-bc4b-42e78941c14b
NDC68788-6882
Product TypeHuman Prescription Drug
Proprietary NameValsartan
Generic NameValsartan
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-01-19
Marketing CategoryANDA / ANDA
Application NumberANDA203311
Labeler NamePreferred Pharmaceuticals Inc.
Substance NameVALSARTAN
Active Ingredient Strength320 mg/1
Pharm ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 68788-6882-9

90 TABLET, FILM COATED in 1 BOTTLE (68788-6882-9)
Marketing Start Date2017-01-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-6882-6 [68788688206]

Valsartan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203311
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-01-19
Marketing End Date2019-11-14

NDC 68788-6882-3 [68788688203]

Valsartan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203311
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-01-19
Marketing End Date2019-11-14

NDC 68788-6882-2 [68788688202]

Valsartan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203311
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-01-19
Marketing End Date2019-11-14

NDC 68788-6882-8 [68788688208]

Valsartan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203311
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-01-19
Marketing End Date2019-11-14

NDC 68788-6882-9 [68788688209]

Valsartan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203311
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-01-19
Marketing End Date2019-11-14

NDC 68788-6882-1 [68788688201]

Valsartan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203311
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-01-19
Marketing End Date2019-11-14

Drug Details

Active Ingredients

IngredientStrength
VALSARTAN320 mg/1

OpenFDA Data

SPL SET ID:fe3a18ca-1f3a-40d2-bc4b-42e78941c14b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 349200
  • Pharmacological Class

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