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NDC 69117-0010-01 Valacyclovir 500 mg/1 Details

Valacyclovir 500 mg/1

Valacyclovir is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Yiling Pharmaceutical, Inc.. The primary component is VALACYCLOVIR HYDROCHLORIDE.

MedlinePlus Drug Summary

Valacyclovir is used to treat herpes zoster (shingles) and genital herpes. It does not cure herpes infections but decreases pain and itching, helps sores to heal, and prevents new ones from forming. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 69117-0010-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Valacyclovir

Product Information

NDC	69117-0010
Product ID	69117-0010_0da6b94c-7d16-2385-e063-6394a90ad5b3
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Valacyclovir
Proprietary Name Suffix	n/a
Non-Proprietary Name	Valacyclovir
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	VALACYCLOVIR HYDROCHLORIDE
Labeler Name	Yiling Pharmaceutical, Inc.
Pharmaceutical Class	DNA Polymerase Inhibitors [MoA], Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA209553
Listing Certified Through	2024-12-31

Package

NDC 69117-0010-01 (69117001001)

Pricing Information	N/A
NDC Package Code	69117-0010-1
Billing NDC	69117001001
Package	30 TABLET in 1 BOTTLE (69117-0010-1)
Marketing Start Date	2018-10-01
NDC Exclude Flag	N