Product NDC: | 0143-9744 |
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): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0143-9744 |
Labeler Name: | West-ward Pharmaceutical Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078629 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091223 |
Package NDC: | 0143-9744-01 |
Package Description: | 1 mL in 1 VIAL, SINGLE-USE (0143-9744-01) |
NDC Code | 0143-9744-01 |
Proprietary Name | Granisetron Hydrochloride |
Package Description | 1 mL in 1 VIAL, SINGLE-USE (0143-9744-01) |
Product NDC | 0143-9744 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Granisetron Hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20091223 |
Marketing Category Name | ANDA |
Labeler Name | West-ward Pharmaceutical Corp |
Substance Name | GRANISETRON HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |