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ondansetron hydrochloride
ondansetron hydrochloride - 55111-156-05 - (ondansetron hydrochloride)
Drug Information of ondansetron hydrochloride
| Product NDC: | 55111-156 |
| Proprietary Name: | ondansetron hydrochloride |
| Non Proprietary Name: | ondansetron hydrochloride |
| Active Ingredient(s): | 24 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: | 55111-156 |
| Labeler Name: | Dr.Reddy's Laboratories Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076183 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20061226 |
Package Information of ondansetron hydrochloride
| Package NDC: | 55111-156-05 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE (55111-156-05) |
NDC Information of ondansetron hydrochloride
| NDC Code | 55111-156-05 |
| Proprietary Name | ondansetron hydrochloride |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (55111-156-05) |
| Product NDC | 55111-156 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ondansetron hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20061226 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr.Reddy's Laboratories Limited |
| Substance Name | ONDANSETRON HYDROCHLORIDE |
| Strength Number | 24 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
