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Oxycodone and Acetaminophen
Oxycodone and Acetaminophen - 21695-619-40 - (Oxycodone and Acetaminophen)
Drug Information of Oxycodone and Acetaminophen
| Product NDC: | 21695-619 |
| Proprietary Name: | Oxycodone and Acetaminophen |
| Non Proprietary Name: | Oxycodone and Acetaminophen |
| Active Ingredient(s): | 325; 10 mg/1; mg/1 & nbsp; Oxycodone and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxycodone and Acetaminophen
| Product NDC: | 21695-619 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040778 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071127 |
Package Information of Oxycodone and Acetaminophen
| Package NDC: | 21695-619-40 |
| Package Description: | 40 TABLET in 1 BOTTLE (21695-619-40) |
NDC Information of Oxycodone and Acetaminophen
| NDC Code | 21695-619-40 |
| Proprietary Name | Oxycodone and Acetaminophen |
| Package Description | 40 TABLET in 1 BOTTLE (21695-619-40) |
| Product NDC | 21695-619 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxycodone and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20071127 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | ACETAMINOPHEN; OXYCODONE |
| Strength Number | 325; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
