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Acyclovir

NDC 51655-679, Acyclovir, tablet, from Northwind Health Company, LLC.

Product NDC
51655-679
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203834
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-679 \
  -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
51655-679-355165506793535 TABLET in 1 BOTTLE, PLASTIC (51655-679-35)
51655-679-515165506795140 TABLET in 1 BOTTLE, PLASTIC (51655-679-51)
51655-679-525165506795230 TABLET in 1 BOTTLE, PLASTIC (51655-679-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f6f56143-ea74-af87-e053-6394a90ae346

Use it

Look up 51655-679 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-679 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-679. 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.