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Xolox
Xolox - 21695-924-40 - (Oxycodone HCl and Acetaminophen)
Drug Information of Xolox
| Product NDC: | 21695-924 |
| Proprietary Name: | Xolox |
| Non Proprietary Name: | Oxycodone HCl and Acetaminophen |
| Active Ingredient(s): | 500; 10 mg/1; mg/1 & nbsp; Oxycodone HCl and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Xolox
| Product NDC: | 21695-924 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040676 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090301 |
Package Information of Xolox
| Package NDC: | 21695-924-40 |
| Package Description: | 40 TABLET in 1 BOTTLE (21695-924-40) |
NDC Information of Xolox
| NDC Code | 21695-924-40 |
| Proprietary Name | Xolox |
| Package Description | 40 TABLET in 1 BOTTLE (21695-924-40) |
| Product NDC | 21695-924 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxycodone HCl and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090301 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
| Strength Number | 500; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
