Home
>
National Drug Code (NDC)
>
OxyContin
OxyContin - 43063-244-30 - (oxycodone hydrochloride)
Drug Information of OxyContin
| Product NDC: | 43063-244 |
| Proprietary Name: | OxyContin |
| Non Proprietary Name: | oxycodone hydrochloride |
| Active Ingredient(s): | 80 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: | 43063-244 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020553 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970101 |
Package Information of OxyContin
| Package NDC: | 43063-244-30 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-244-30) |
NDC Information of OxyContin
| NDC Code | 43063-244-30 |
| Proprietary Name | OxyContin |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-244-30) |
| Product NDC | 43063-244 |
| 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 | 19970101 |
| Marketing Category Name | NDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
