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ONDANSETRON
ONDANSETRON - 62756-356-64 - (ONDANSETRON)
Drug Information of ONDANSETRON
| Product NDC: | 62756-356 |
| Proprietary Name: | ONDANSETRON |
| Non Proprietary Name: | ONDANSETRON |
| Active Ingredient(s): | 8 mg/1 & nbsp; ONDANSETRON |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ONDANSETRON
| Product NDC: | 62756-356 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077557 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070802 |
Package Information of ONDANSETRON
| Package NDC: | 62756-356-64 |
| Package Description: | 3 BLISTER PACK in 1 DOSE PACK (62756-356-64) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Information of ONDANSETRON
| NDC Code | 62756-356-64 |
| Proprietary Name | ONDANSETRON |
| Package Description | 3 BLISTER PACK in 1 DOSE PACK (62756-356-64) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 62756-356 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ONDANSETRON |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20070802 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | ONDANSETRON |
| Strength Number | 8 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
