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OXYCODONE AND ACETAMINOPHEN
OXYCODONE AND ACETAMINOPHEN - 49999-854-30 - (oxycodone hydrochloride and acetaminophen)
Drug Information of OXYCODONE AND ACETAMINOPHEN
| Product NDC: | 49999-854 |
| 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: | 49999-854 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040545 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110201 |
Package Information of OXYCODONE AND ACETAMINOPHEN
| Package NDC: | 49999-854-30 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (49999-854-30) |
NDC Information of OXYCODONE AND ACETAMINOPHEN
| NDC Code | 49999-854-30 |
| Proprietary Name | OXYCODONE AND ACETAMINOPHEN |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (49999-854-30) |
| Product NDC | 49999-854 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxycodone hydrochloride and acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110201 |
| Marketing Category Name | ANDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
| Strength Number | 325; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
