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OxyContin
OxyContin - 54868-5966-0 - (oxycodone hydrochloride)
Drug Information of OxyContin
| Product NDC: | 54868-5966 |
| Proprietary Name: | OxyContin |
| Non Proprietary Name: | oxycodone hydrochloride |
| Active Ingredient(s): | 30 mg/1 & nbsp; oxycodone hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OxyContin
| Product NDC: | 54868-5966 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022272 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100808 |
Package Information of OxyContin
| Package NDC: | 54868-5966-0 |
| Package Description: | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5966-0) |
NDC Information of OxyContin
| NDC Code | 54868-5966-0 |
| Proprietary Name | OxyContin |
| Package Description | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5966-0) |
| Product NDC | 54868-5966 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxycodone hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100808 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
