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Qsymia
Qsymia - 62541-202-30 - (phentermine hydrochloride and topiramate)
Drug Information of Qsymia
| Product NDC: | 62541-202 |
| Proprietary Name: | Qsymia |
| Non Proprietary Name: | phentermine hydrochloride and topiramate |
| Active Ingredient(s): | 7.5; 46 mg/1; mg/1 & nbsp; phentermine hydrochloride and topiramate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Qsymia
| Product NDC: | 62541-202 |
| Labeler Name: | Vivus, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022580 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120918 |
Package Information of Qsymia
| Package NDC: | 62541-202-30 |
| Package Description: | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, UNIT-DOSE (62541-202-30) |
NDC Information of Qsymia
| NDC Code | 62541-202-30 |
| Proprietary Name | Qsymia |
| Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, UNIT-DOSE (62541-202-30) |
| Product NDC | 62541-202 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | phentermine hydrochloride and topiramate |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120918 |
| Marketing Category Name | NDA |
| Labeler Name | Vivus, Inc. |
| Substance Name | PHENTERMINE HYDROCHLORIDE; TOPIRAMATE |
| Strength Number | 7.5; 46 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC],Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
