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Acyclovir

NDC 71205-053, Acyclovir, tablet, from Proficient Rx LP.

Product NDC
71205-053
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075382
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-053 \
  -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
71205-053-307120500533030 TABLET in 1 BOTTLE, PLASTIC (71205-053-30)
71205-053-357120500533535 TABLET in 1 BOTTLE, PLASTIC (71205-053-35)
71205-053-607120500536060 TABLET in 1 BOTTLE, PLASTIC (71205-053-60)
71205-053-907120500539090 TABLET in 1 BOTTLE, PLASTIC (71205-053-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/33630a35-346e-43b6-9286-89e28ac0094a

Use it

Look up 71205-053 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-053 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-053. 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.