Search by Drug Name or NDC
NDC 71335-0708-06 Valacyclovir Hydrochloride 500 mg/1 Details
Valacyclovir Hydrochloride 500 mg/1
Valacyclovir Hydrochloride 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 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: 71335-0708-06Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Valacyclovir
Product Information
| NDC | 71335-0708 |
|---|---|
| Product ID | 71335-0708_23d2bf71-d94e-4dc2-9a27-921d0c7f1ea7 |
| Associated GPIs | 12405085100310 |
| GCN Sequence Number | 023989 |
| GCN Sequence Number Description | valacyclovir HCl TABLET 500 MG ORAL |
| HIC3 | W5A |
| HIC3 Description | ANTIVIRALS, GENERAL |
| GCN | 13740 |
| HICL Sequence Number | 010117 |
| HICL Sequence Number Description | VALACYCLOVIR HCL |
| Brand/Generic | Generic |
| Proprietary Name | Valacyclovir Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Valacyclovir Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 500 |
| Active Ingredient Units | mg/1 |
| Substance Name | VALACYCLOVIR HYDROCHLORIDE |
| Labeler Name | Bryant Ranch Prepack |
| 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 | ANDA090682 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 71335-0708-06 (71335070806)
| NDC Package Code | 71335-0708-6 |
|---|---|
| Billing NDC | 71335070806 |
| Package | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0708-6) |
| Marketing Start Date | 2018-02-26 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |