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Granisetron hydrochloride

NDC 63850-0005, Granisetron hydrochloride, tablet, film coated, from Natco Pharma Limited.

Product NDC
63850-0005
Status
Listed
Labeler
Natco Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078969
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63850-0005 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GRANISETRON HYDROCHLORIDE1 mg/1

Pharmacologic classes

Serotonin 3 Receptor Antagonists [MoA]; Serotonin-3 Receptor Antagonist [EPC]

Package NDCNDC-11Package
63850-0005-16385000050110 TABLET, FILM COATED in 1 BLISTER PACK (63850-0005-1)
63850-0005-2638500005022 TABLET, FILM COATED in 1 BLISTER PACK (63850-0005-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d2be8de3-04fe-4e92-82b4-98d749b89596

Use it

Look up 63850-0005 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63850-0005 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63850-0005. 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.