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Famciclovir

NDC 71205-609, Famciclovir, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-609
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201022
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-609 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMCICLOVIR500 mg/1

Pharmacologic classes

DNA Polymerase Inhibitors [MoA]; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]; Nucleoside Analog [EXT]

Package NDCNDC-11Package
71205-609-217120506092121 TABLET, FILM COATED in 1 BOTTLE (71205-609-21)
71205-609-307120506093030 TABLET, FILM COATED in 1 BOTTLE (71205-609-30)
71205-609-607120506096060 TABLET, FILM COATED in 1 BOTTLE (71205-609-60)
71205-609-907120506099090 TABLET, FILM COATED in 1 BOTTLE (71205-609-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b75abffb-0a90-4abd-8ed8-81be1d8fe364

Use it

Look up 71205-609 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-609 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-609. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.