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Valacyclovir

NDC 70518-2402, Valacyclovir, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-2402
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203047
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2402 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VALACYCLOVIR HYDROCHLORIDE1 g/1

Pharmacologic classes

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 [EXT]

Package NDCNDC-11Package
70518-2402-7705182402077 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2402-7)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7c332401-afb6-455b-b61a-ea108a377ef6

Use it

Look up 70518-2402 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2402 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2402. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.