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GRANISETRON HYDROCHLORIDE
GRANISETRON HYDROCHLORIDE - 64720-198-97 - (GRANISETRON HYDROCHLORIDE)
Drug Information of GRANISETRON HYDROCHLORIDE
| Product NDC: | 64720-198 |
| 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: | 64720-198 |
| Labeler Name: | COREPHARMA LLC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078260 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071231 |
Package Information of GRANISETRON HYDROCHLORIDE
| Package NDC: | 64720-198-97 |
| Package Description: | 20 TABLET, FILM COATED in 1 BLISTER PACK (64720-198-97) |
NDC Information of GRANISETRON HYDROCHLORIDE
| NDC Code | 64720-198-97 |
| Proprietary Name | GRANISETRON HYDROCHLORIDE |
| Package Description | 20 TABLET, FILM COATED in 1 BLISTER PACK (64720-198-97) |
| Product NDC | 64720-198 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GRANISETRON HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20071231 |
| Marketing Category Name | ANDA |
| Labeler Name | COREPHARMA LLC. |
| Substance Name | GRANISETRON HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
