Granisetron Hydrochloride
- Product NDC
- 0054-0143
- 11-digit product format
- 000540143
- Labeler code
- 0054
- Product ID
- 0054-0143_ee04cf79-6c59-4574-a3e0-6843f78917c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Granisetron Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- West-Ward Pharmaceuticals Corp.
- Application
- ANDA077842
- Marketing category
- ANDA
- Marketing start
- 2007-12-31
- Marketing end
- 0000-00-00
- Substance
- GRANISETRON HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0054-0143-07 | 00054014307 | 20 TABLET in 1 BOTTLE (0054-0143-07) | 20 tablet | 2008-11-24 | 0000-00-00 | No | No | Current |
| 0054-0143-08 | 00054014308 | 10 BLISTER PACK in 1 CARTON (0054-0143-08) > 2 TABLET in 1 BLISTER PACK | 10 blister pack | 2007-12-31 | 0000-00-00 | No | No | Current |
| 0054-0143-87 | 00054014387 | 2 TABLET in 1 BOTTLE (0054-0143-87) | 2 tablet | 2008-11-24 | 0000-00-00 | No | No | Current |