Product NDC: | 68405-380 |
Proprietary Name: | Theratramadol-60 |
Non Proprietary Name: | TRAMADOL HYDROCHLORIDE, GABA |
Active Ingredient(s): | & nbsp; TRAMADOL HYDROCHLORIDE, GABA |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68405-380 |
Labeler Name: | Physician Therapeutics LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110520 |
Package NDC: | 68405-380-26 |
Package Description: | 1 KIT in 1 KIT (68405-380-26) * 60 TABLET in 1 BOTTLE (52959-688-60) * 60 CAPSULE in 1 BOTTLE |
NDC Code | 68405-380-26 |
Proprietary Name | Theratramadol-60 |
Package Description | 1 KIT in 1 KIT (68405-380-26) * 60 TABLET in 1 BOTTLE (52959-688-60) * 60 CAPSULE in 1 BOTTLE |
Product NDC | 68405-380 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | TRAMADOL HYDROCHLORIDE, GABA |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20110520 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Physician Therapeutics LLC |
Substance Name | |
Strength Number | |
Strength Unit | |
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