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Acyclovir

NDC 71209-005, Acyclovir, tablet, from Cadila Pharmaceuticals Limited.

Product NDC
71209-005
Status
Listed
Labeler
Cadila Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202168
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71209-005 \
  -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
71209-005-0571209000505100 TABLET in 1 BOTTLE (71209-005-05)
71209-005-1071209000510500 TABLET in 1 BOTTLE (71209-005-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/acef88f4-6456-4092-993f-27e1496097c7

Use it

Look up 71209-005 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71209-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71209-005. 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.