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Theratramadol-90
Theratramadol-90 - 68405-038-36 - (TRAMADOL HYDROCHLORIDE, .GAMMA.-AMINOBUTYRIC ACID)
Drug Information of Theratramadol-90
| Product NDC: | 68405-038 |
| Proprietary Name: | Theratramadol-90 |
| Non Proprietary Name: | TRAMADOL HYDROCHLORIDE, .GAMMA.-AMINOBUTYRIC ACID |
| Active Ingredient(s): | & nbsp; TRAMADOL HYDROCHLORIDE, .GAMMA.-AMINOBUTYRIC ACID |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Theratramadol-90
| Product NDC: | 68405-038 |
| Labeler Name: | Physician Therapeutics LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110204 |
Package Information of Theratramadol-90
| Package NDC: | 68405-038-36 |
| Package Description: | 1 KIT in 1 KIT (68405-038-36) * 60 TABLET in 1 BOTTLE (52959-688-60) * 90 CAPSULE in 1 BOTTLE |
NDC Information of Theratramadol-90
| NDC Code | 68405-038-36 |
| Proprietary Name | Theratramadol-90 |
| Package Description | 1 KIT in 1 KIT (68405-038-36) * 60 TABLET in 1 BOTTLE (52959-688-60) * 90 CAPSULE in 1 BOTTLE |
| Product NDC | 68405-038 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TRAMADOL HYDROCHLORIDE, .GAMMA.-AMINOBUTYRIC ACID |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110204 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Physician Therapeutics LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
