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OXECTA
OXECTA - 60793-526-01 - (OXYCODONE HYDROCHLORIDE)
Drug Information of OXECTA
| Product NDC: | 60793-526 |
| Proprietary Name: | OXECTA |
| Non Proprietary Name: | OXYCODONE HYDROCHLORIDE |
| Active Ingredient(s): | 7.5 mg/1 & nbsp; OXYCODONE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OXECTA
| Product NDC: | 60793-526 |
| Labeler Name: | King Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA202080 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110617 |
Package Information of OXECTA
| Package NDC: | 60793-526-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (60793-526-01) |
NDC Information of OXECTA
| NDC Code | 60793-526-01 |
| Proprietary Name | OXECTA |
| Package Description | 100 TABLET in 1 BOTTLE (60793-526-01) |
| Product NDC | 60793-526 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | OXYCODONE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110617 |
| Marketing Category Name | NDA |
| Labeler Name | King Pharmaceuticals, Inc. |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 7.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
