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acyclovir

NDC 71205-391, acyclovir, tablet, from Proficient Rx LP.

Product NDC
71205-391
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077309
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-391 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACYCLOVIR400 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
71205-391-257120503912525 TABLET in 1 BOTTLE (71205-391-25)
71205-391-307120503913030 TABLET in 1 BOTTLE (71205-391-30)
71205-391-607120503916060 TABLET in 1 BOTTLE (71205-391-60)
71205-391-907120503919090 TABLET in 1 BOTTLE (71205-391-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/51052f0e-1a07-405a-a962-981ce9439e02

Use it

Look up 71205-391 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-391 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-391. 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.