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Granisetron
Granisetron - 63323-319-04 - (GRANISETRON HYDROCHLORIDE)
Drug Information of Granisetron
| Product NDC: | 63323-319 |
| Proprietary Name: | Granisetron |
| Non Proprietary Name: | GRANISETRON HYDROCHLORIDE |
| Active Ingredient(s): | 1 mg/mL & nbsp; GRANISETRON HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Granisetron
| Product NDC: | 63323-319 |
| Labeler Name: | Fresenius Kabi USA, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078090 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091120 |
Package Information of Granisetron
| Package NDC: | 63323-319-04 |
| Package Description: | 1 VIAL in 1 BOX (63323-319-04) > 4 mL in 1 VIAL |
NDC Information of Granisetron
| NDC Code | 63323-319-04 |
| Proprietary Name | Granisetron |
| Package Description | 1 VIAL in 1 BOX (63323-319-04) > 4 mL in 1 VIAL |
| Product NDC | 63323-319 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GRANISETRON HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20091120 |
| Marketing Category Name | ANDA |
| Labeler Name | Fresenius Kabi USA, LLC |
| Substance Name | GRANISETRON HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
