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Trezix
Trezix - 66992-340-10 - (acetaminophen, caffeine, dihydrocodeine bitartrate)
Drug Information of Trezix
| Product NDC: | 66992-340 |
| Proprietary Name: | Trezix |
| Non Proprietary Name: | acetaminophen, caffeine, dihydrocodeine bitartrate |
| Active Ingredient(s): | 320.5; 30; 16 mg/1; mg/1; mg/1 & nbsp; acetaminophen, caffeine, dihydrocodeine bitartrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Trezix
| Product NDC: | 66992-340 |
| Labeler Name: | WraSer LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040688 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090901 |
Package Information of Trezix
| Package NDC: | 66992-340-10 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (66992-340-10) |
NDC Information of Trezix
| NDC Code | 66992-340-10 |
| Proprietary Name | Trezix |
| Package Description | 100 CAPSULE in 1 BOTTLE (66992-340-10) |
| Product NDC | 66992-340 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acetaminophen, caffeine, dihydrocodeine bitartrate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | ANDA |
| Labeler Name | WraSer LLC |
| Substance Name | ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE |
| Strength Number | 320.5; 30; 16 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient],Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
