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Ondansetron hydrochloride and dextrose
Ondansetron hydrochloride and dextrose - 0069-0700-12 - (ondansetron hydrochloride and dextrose)
Drug Information of Ondansetron hydrochloride and dextrose
| Product NDC: | 0069-0700 |
| Proprietary Name: | Ondansetron hydrochloride and dextrose |
| Non Proprietary Name: | ondansetron hydrochloride and dextrose |
| Active Ingredient(s): | 32 mg/50mL & nbsp; ondansetron hydrochloride and dextrose |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ondansetron hydrochloride and dextrose
| Product NDC: | 0069-0700 |
| Labeler Name: | Pfizer Labs, Division of Pfizer Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078308 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090501 |
Package Information of Ondansetron hydrochloride and dextrose
| Package NDC: | 0069-0700-12 |
| Package Description: | 6 BAG in 1 CASE (0069-0700-12) > 50 mL in 1 BAG |
NDC Information of Ondansetron hydrochloride and dextrose
| NDC Code | 0069-0700-12 |
| Proprietary Name | Ondansetron hydrochloride and dextrose |
| Package Description | 6 BAG in 1 CASE (0069-0700-12) > 50 mL in 1 BAG |
| Product NDC | 0069-0700 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ondansetron hydrochloride and dextrose |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090501 |
| Marketing Category Name | ANDA |
| Labeler Name | Pfizer Labs, Division of Pfizer Inc. |
| Substance Name | ONDANSETRON HYDROCHLORIDE |
| Strength Number | 32 |
| Strength Unit | mg/50mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
