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OXYCODONE AND ACETAMINOPHEN
OXYCODONE AND ACETAMINOPHEN - 63629-3953-6 - (Oxycodone hydrochloride and Acetaminophen)
Drug Information of OXYCODONE AND ACETAMINOPHEN
| Product NDC: | 63629-3953 |
| Proprietary Name: | OXYCODONE AND ACETAMINOPHEN |
| Non Proprietary Name: | Oxycodone hydrochloride and Acetaminophen |
| Active Ingredient(s): | 325; 10 mg/1; mg/1 & nbsp; Oxycodone hydrochloride and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OXYCODONE AND ACETAMINOPHEN
| Product NDC: | 63629-3953 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090177 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090806 |
Package Information of OXYCODONE AND ACETAMINOPHEN
| Package NDC: | 63629-3953-6 |
| Package Description: | 20 TABLET in 1 BOTTLE (63629-3953-6) |
NDC Information of OXYCODONE AND ACETAMINOPHEN
| NDC Code | 63629-3953-6 |
| Proprietary Name | OXYCODONE AND ACETAMINOPHEN |
| Package Description | 20 TABLET in 1 BOTTLE (63629-3953-6) |
| Product NDC | 63629-3953 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxycodone hydrochloride and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090806 |
| Marketing Category Name | ANDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
| Strength Number | 325; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
