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GRANISETRON HYDROCHLORIDE
GRANISETRON HYDROCHLORIDE - 55648-662-01 - (GRANISETRON HYDROCHLORIDE)
Drug Information of GRANISETRON HYDROCHLORIDE
| Product NDC: | 55648-662 |
| 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: | 55648-662 |
| Labeler Name: | WOCKHARDT LIMITED |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078566 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080303 |
Package Information of GRANISETRON HYDROCHLORIDE
| Package NDC: | 55648-662-01 |
| Package Description: | 5 CARTON in 1 CARTON (55648-662-01) > 1 VIAL, SINGLE-USE in 1 CARTON (55648-662-02) > 1 mL in 1 VIAL, SINGLE-USE |
NDC Information of GRANISETRON HYDROCHLORIDE
| NDC Code | 55648-662-01 |
| Proprietary Name | GRANISETRON HYDROCHLORIDE |
| Package Description | 5 CARTON in 1 CARTON (55648-662-01) > 1 VIAL, SINGLE-USE in 1 CARTON (55648-662-02) > 1 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 55648-662 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GRANISETRON HYDROCHLORIDE |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20080303 |
| Marketing Category Name | ANDA |
| Labeler Name | WOCKHARDT LIMITED |
| Substance Name | GRANISETRON HYDROCHLORIDE |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
