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Granisetron Hydrochloride
Granisetron Hydrochloride - 16714-221-30 - (Granisetron Hydrochloride)
Drug Information of Granisetron Hydrochloride
| Product NDC: | 16714-221 |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Granisetron Hydrochloride
| Product NDC: | 16714-221 |
| Labeler Name: | Northstar Rx LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078678 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080429 |
Package Information of Granisetron Hydrochloride
| Package NDC: | 16714-221-30 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (16714-221-30) > 1 TABLET, FILM COATED in 1 BLISTER PACK (16714-221-10) |
NDC Information of Granisetron Hydrochloride
| NDC Code | 16714-221-30 |
| Proprietary Name | Granisetron Hydrochloride |
| Package Description | 2 BLISTER PACK in 1 CARTON (16714-221-30) > 1 TABLET, FILM COATED in 1 BLISTER PACK (16714-221-10) |
| Product NDC | 16714-221 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Granisetron Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20080429 |
| Marketing Category Name | ANDA |
| Labeler Name | Northstar Rx LLC |
| Substance Name | GRANISETRON HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
