NDC 67877-418

Valsartan

Valsartan

Valsartan is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Ascend Laboratories, Llc. The primary component is Valsartan.

Product ID67877-418_205dbc75-b804-4b40-85ee-3c2d9de93de0
NDC67877-418
Product TypeHuman Prescription Drug
Proprietary NameValsartan
Generic NameValsartan
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2019-03-14
Marketing CategoryANDA / ANDA
Application NumberANDA205536
Labeler NameAscend Laboratories, LLC
Substance NameVALSARTAN
Active Ingredient Strength320 mg/1
Pharm ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 67877-418-05

500 TABLET, FILM COATED in 1 BOTTLE (67877-418-05)
Marketing Start Date2019-03-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67877-418-10 [67877041810]

Valsartan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA205536
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-03-14

NDC 67877-418-90 [67877041890]

Valsartan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA205536
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-03-14

NDC 67877-418-05 [67877041805]

Valsartan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA205536
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-03-14

Drug Details

Active Ingredients

IngredientStrength
VALSARTAN320 mg/1

OpenFDA Data

SPL SET ID:7b4ecaf9-e84c-4660-9cd1-65a238efd8a8
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 349483
  • 349201
  • 349200
  • 349199
  • UPC Code
  • 0367877415307
  • Pharmacological Class

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