Home
>
National Drug Code (NDC)
>
OxyContin
OxyContin - 49999-856-60 - (oxycodone hydrochloride)
Drug Information of OxyContin
| Product NDC: | 49999-856 |
| Proprietary Name: | OxyContin |
| Non Proprietary Name: | oxycodone hydrochloride |
| Active Ingredient(s): | 40 kg/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: | 49999-856 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022272 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19951201 |
Package Information of OxyContin
| Package NDC: | 49999-856-60 |
| Package Description: | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49999-856-60) |
NDC Information of OxyContin
| NDC Code | 49999-856-60 |
| Proprietary Name | OxyContin |
| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49999-856-60) |
| Product NDC | 49999-856 |
| 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 | 19951201 |
| Marketing Category Name | NDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 40 |
| Strength Unit | kg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
