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Granisetron hydrochloride
Granisetron hydrochloride - 55390-250-10 - (Granisetron hydrochloride)
Drug Information of Granisetron hydrochloride
| Product NDC: | 55390-250 |
| Proprietary Name: | Granisetron hydrochloride |
| Non Proprietary Name: | Granisetron hydrochloride |
| Active Ingredient(s): | .112 mg/mL & nbsp; Granisetron hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Granisetron hydrochloride
| Product NDC: | 55390-250 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077913 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080728 |
Package Information of Granisetron hydrochloride
| Package NDC: | 55390-250-10 |
| Package Description: | 10 VIAL in 1 BOX (55390-250-10) > 1 mL in 1 VIAL |
NDC Information of Granisetron hydrochloride
| NDC Code | 55390-250-10 |
| Proprietary Name | Granisetron hydrochloride |
| Package Description | 10 VIAL in 1 BOX (55390-250-10) > 1 mL in 1 VIAL |
| Product NDC | 55390-250 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Granisetron hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20080728 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | GRANISETRON HYDROCHLORIDE |
| Strength Number | .112 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
