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Appbutamone-D
Appbutamone-D - 68405-009-16 - (BUPROPION HYDROCHLORIDE, TYROSINE)
Drug Information of Appbutamone-D
| Product NDC: | 68405-009 |
| Proprietary Name: | Appbutamone-D |
| Non Proprietary Name: | BUPROPION HYDROCHLORIDE, TYROSINE |
| Active Ingredient(s): | & nbsp; BUPROPION HYDROCHLORIDE, TYROSINE |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Appbutamone-D
| Product NDC: | 68405-009 |
| 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 Appbutamone-D
| Package NDC: | 68405-009-16 |
| Package Description: | 1 KIT in 1 KIT (68405-009-16) * 30 TABLET in 1 BOTTLE (52959-898-30) * 120 CAPSULE in 1 BOTTLE |
NDC Information of Appbutamone-D
| NDC Code | 68405-009-16 |
| Proprietary Name | Appbutamone-D |
| Package Description | 1 KIT in 1 KIT (68405-009-16) * 30 TABLET in 1 BOTTLE (52959-898-30) * 120 CAPSULE in 1 BOTTLE |
| Product NDC | 68405-009 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | BUPROPION HYDROCHLORIDE, TYROSINE |
| 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 |
