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Ondansetron Hydrochloride
Ondansetron Hydrochloride - 0093-7236-93 - (Ondansetron Hydrochloride)
Drug Information of Ondansetron Hydrochloride
| Product NDC: | 0093-7236 |
| Proprietary Name: | Ondansetron Hydrochloride |
| Non Proprietary Name: | Ondansetron Hydrochloride |
| Active Ingredient(s): | 8 mg/1 & nbsp; Ondansetron Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ondansetron Hydrochloride
| Product NDC: | 0093-7236 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076252 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070703 |
Package Information of Ondansetron Hydrochloride
| Package NDC: | 0093-7236-93 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0093-7236-93) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-7236-19) |
NDC Information of Ondansetron Hydrochloride
| NDC Code | 0093-7236-93 |
| Proprietary Name | Ondansetron Hydrochloride |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0093-7236-93) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-7236-19) |
| Product NDC | 0093-7236 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ondansetron Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070703 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | ONDANSETRON HYDROCHLORIDE |
| Strength Number | 8 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
