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
- 51991-735_1919cca7-47e5-4474-8ad1-a49275d4f85b
- Product NDC
- 51991-735
- Form
- TABLET
- Composition / generic term
- Granisetron Hydrochloride
- Labeler
- Breckenridge Pharmaceutical, Inc.
- 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
- 2 BLISTER PACK in 1 CARTON (51991-735-20) / 10 TABLET in 1 BLISTER PACK · 51991-735-20
- 1 BLISTER PACK in 1 CARTON (51991-735-32) / 2 TABLET in 1 BLISTER PACK · 51991-735-32
Source and coverage
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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.
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