| Product NDC: | 65224-707 |
| Proprietary Name: | Omeclamox-Pak |
| Non Proprietary Name: | omeprazole, clarithromycin, amoxicillin |
| Active Ingredient(s): | & nbsp; omeprazole, clarithromycin, amoxicillin |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65224-707 |
| Labeler Name: | Pernix Therapeutics, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050824 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120427 |
| Package NDC: | 65224-707-11 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (65224-707-11) > 1 KIT in 1 BLISTER PACK |
| NDC Code | 65224-707-11 |
| Proprietary Name | Omeclamox-Pak |
| Package Description | 10 BLISTER PACK in 1 CARTON (65224-707-11) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 65224-707 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | omeprazole, clarithromycin, amoxicillin |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20120427 |
| Marketing Category Name | NDA |
| Labeler Name | Pernix Therapeutics, LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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