United States · FDA National Drug Code directory
Granisetron hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 63850-0005_67953305-4eb0-4b00-abae-716ac25c5bf9
- Product NDC
- 63850-0005
- Form
- TABLET, FILM COATED
- Composition / generic term
- Granisetron hydrochloride
- Labeler
- Natco Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090622
- Source listing expiry
- 20261231
Source-listed ingredients
- GRANISETRON HYDROCHLORIDE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, FILM COATED in 1 BLISTER PACK (63850-0005-1) · 63850-0005-1
- 2 TABLET, FILM COATED in 1 BLISTER PACK (63850-0005-2) · 63850-0005-2
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →