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ACYCLOVIR

NDC 70518-4186, ACYCLOVIR, tablet, from REMEDYREPACK INC..

Product NDC
70518-4186
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074891
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4186 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACYCLOVIR800 mg/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
70518-4186-07051841860010 TABLET in 1 BOTTLE, PLASTIC (70518-4186-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c1744e01-0e40-4851-8ffc-c3bf29dd7c2b

Use it

Look up 70518-4186 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4186 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4186. 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.