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granisetron hydrochloride
granisetron hydrochloride - 25021-778-01 - (granisetron hydrochloride)
Drug Information of granisetron hydrochloride
| Product NDC: | 25021-778 |
| 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: | 25021-778 |
| Labeler Name: | Sagent Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091136 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101201 |
Package Information of granisetron hydrochloride
| Package NDC: | 25021-778-01 |
| Package Description: | 5 VIAL in 1 CARTON (25021-778-01) > 1 mL in 1 VIAL |
NDC Information of granisetron hydrochloride
| NDC Code | 25021-778-01 |
| Proprietary Name | granisetron hydrochloride |
| Package Description | 5 VIAL in 1 CARTON (25021-778-01) > 1 mL in 1 VIAL |
| Product NDC | 25021-778 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | granisetron hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20101201 |
| Marketing Category Name | ANDA |
| Labeler Name | Sagent Pharmaceuticals |
| Substance Name | GRANISETRON HYDROCHLORIDE |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
