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Zofran
Zofran - 49349-858-08 - (Ondansetron Hydrochloride)
Drug Information of Zofran
| Product NDC: | 49349-858 |
| Proprietary Name: | Zofran |
| Non Proprietary Name: | Ondansetron Hydrochloride |
| Active Ingredient(s): | 8 mg/1 & nbsp; Ondansetron Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zofran
| Product NDC: | 49349-858 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020781 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20111219 |
Package Information of Zofran
| Package NDC: | 49349-858-08 |
| Package Description: | 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49349-858-08) |
NDC Information of Zofran
| NDC Code | 49349-858-08 |
| Proprietary Name | Zofran |
| Package Description | 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49349-858-08) |
| Product NDC | 49349-858 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ondansetron Hydrochloride |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20111219 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | ONDANSETRON HYDROCHLORIDE |
| Strength Number | 8 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
