Product NDC: | 0054-0143 |
Proprietary Name: | Granisetron Hydrochloride |
Non Proprietary Name: | Granisetron Hydrochloride |
Active Ingredient(s): | 1 mg/1 & nbsp; Granisetron Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-0143 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077842 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080516 |
Package NDC: | 0054-0143-08 |
Package Description: | 10 BLISTER PACK in 1 CARTON (0054-0143-08) > 2 TABLET in 1 BLISTER PACK |
NDC Code | 0054-0143-08 |
Proprietary Name | Granisetron Hydrochloride |
Package Description | 10 BLISTER PACK in 1 CARTON (0054-0143-08) > 2 TABLET in 1 BLISTER PACK |
Product NDC | 0054-0143 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Granisetron Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20080516 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | GRANISETRON HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |