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Granisetron
Granisetron - 66758-035-01 - (Granisetron)
Drug Information of Granisetron
| Product NDC: | 66758-035 |
| Proprietary Name: | Granisetron |
| Non Proprietary Name: | Granisetron |
| Active Ingredient(s): | 1 mg/mL & nbsp; Granisetron |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Granisetron
| Product NDC: | 66758-035 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078835 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080630 |
Package Information of Granisetron
| Package NDC: | 66758-035-01 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (66758-035-01) > 1 mL in 1 VIAL, SINGLE-USE |
NDC Information of Granisetron
| NDC Code | 66758-035-01 |
| Proprietary Name | Granisetron |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (66758-035-01) > 1 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 66758-035 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Granisetron |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20080630 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | GRANISETRON HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
