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Xodol
Xodol - 21695-775-60 - (Hydrocodone Bitartrate and Acetaminophen)
Drug Information of Xodol
| Product NDC: | 21695-775 |
| Proprietary Name: | Xodol |
| Non Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
| Active Ingredient(s): | 300; 10 mg/1; mg/1 & nbsp; Hydrocodone Bitartrate and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Xodol
| Product NDC: | 21695-775 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040556 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040623 |
Package Information of Xodol
| Package NDC: | 21695-775-60 |
| Package Description: | 60 TABLET in 1 BOTTLE (21695-775-60) |
NDC Information of Xodol
| NDC Code | 21695-775-60 |
| Proprietary Name | Xodol |
| Package Description | 60 TABLET in 1 BOTTLE (21695-775-60) |
| Product NDC | 21695-775 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040623 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 300; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
