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Granisetron Hydrochloride
Granisetron Hydrochloride - 17478-547-01 - (Granisetron Hydrochloride)
Drug Information of Granisetron Hydrochloride
| Product NDC: | 17478-547 |
| Proprietary Name: | Granisetron Hydrochloride |
| Non Proprietary Name: | Granisetron Hydrochloride |
| Active Ingredient(s): | .1 mg/mL & nbsp; Granisetron Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Granisetron Hydrochloride
| Product NDC: | 17478-547 |
| Labeler Name: | Akorn Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079119 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091001 |
Package Information of Granisetron Hydrochloride
| Package NDC: | 17478-547-01 |
| Package Description: | 10 VIAL, GLASS in 1 CARTON (17478-547-01) > 1 mL in 1 VIAL, GLASS |
NDC Information of Granisetron Hydrochloride
| NDC Code | 17478-547-01 |
| Proprietary Name | Granisetron Hydrochloride |
| Package Description | 10 VIAL, GLASS in 1 CARTON (17478-547-01) > 1 mL in 1 VIAL, GLASS |
| Product NDC | 17478-547 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Granisetron Hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20091001 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn Inc. |
| Substance Name | GRANISETRON HYDROCHLORIDE |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
