Granisetron Hydrochloride
- Product NDC
- 17478-547
- 11-digit product format
- 174780547
- Labeler code
- 17478
- Product ID
- 17478-547_5832d08f-e5e9-4308-859a-3881906212c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Granisetron Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Akorn
- Application
- ANDA079119
- Marketing category
- ANDA
- Marketing start
- 2009-10-01
- Marketing end
- 0000-00-00
- Substance
- GRANISETRON HYDROCHLORIDE
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-547-01 | 17478054701 | 10 VIAL, SINGLE-DOSE in 1 CARTON (17478-547-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2009-10-01 | 0000-00-00 | No | No | Current |