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Gaboxetine
Gaboxetine - 68405-014-26 - (FLUOXETINE HYDROCHLORIDE, CHOLINE)
Drug Information of Gaboxetine
| Product NDC: | 68405-014 |
| Proprietary Name: | Gaboxetine |
| Non Proprietary Name: | FLUOXETINE HYDROCHLORIDE, CHOLINE |
| Active Ingredient(s): | & nbsp; FLUOXETINE HYDROCHLORIDE, CHOLINE |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gaboxetine
| Product NDC: | 68405-014 |
| Labeler Name: | Physician Therapeutics LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110707 |
Package Information of Gaboxetine
| Package NDC: | 68405-014-26 |
| Package Description: | 1 KIT in 1 KIT (68405-014-26) * 30 CAPSULE in 1 BOTTLE (52959-669-30) * 60 CAPSULE in 1 BOTTLE |
NDC Information of Gaboxetine
| NDC Code | 68405-014-26 |
| Proprietary Name | Gaboxetine |
| Package Description | 1 KIT in 1 KIT (68405-014-26) * 30 CAPSULE in 1 BOTTLE (52959-669-30) * 60 CAPSULE in 1 BOTTLE |
| Product NDC | 68405-014 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FLUOXETINE HYDROCHLORIDE, CHOLINE |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110707 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Physician Therapeutics LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
