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Granisol
Granisol - 52547-801-30 - (Granisetron Hydrochloride)
Drug Information of Granisol
| Product NDC: | 52547-801 |
| Proprietary Name: | Granisol |
| Non Proprietary Name: | Granisetron Hydrochloride |
| Active Ingredient(s): | 2 mg/10mL & nbsp; Granisetron Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Granisol
| Product NDC: | 52547-801 |
| Labeler Name: | PediatRx, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078334 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080307 |
Package Information of Granisol
| Package NDC: | 52547-801-30 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (52547-801-30) > 30 mL in 1 BOTTLE, GLASS |
NDC Information of Granisol
| NDC Code | 52547-801-30 |
| Proprietary Name | Granisol |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (52547-801-30) > 30 mL in 1 BOTTLE, GLASS |
| Product NDC | 52547-801 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Granisetron Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20080307 |
| Marketing Category Name | ANDA |
| Labeler Name | PediatRx, Inc. |
| Substance Name | GRANISETRON HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
