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OXYCONTIN
OXYCONTIN - 42549-645-30 - (OXYCODONE HYDROCHLORIDE)
Drug Information of OXYCONTIN
| Product NDC: | 42549-645 |
| Proprietary Name: | OXYCONTIN |
| Non Proprietary Name: | OXYCODONE HYDROCHLORIDE |
| Active Ingredient(s): | 20 mg/1 & nbsp; OXYCODONE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OXYCONTIN
| Product NDC: | 42549-645 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022272 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100808 |
Package Information of OXYCONTIN
| Package NDC: | 42549-645-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (42549-645-30) |
NDC Information of OXYCONTIN
| NDC Code | 42549-645-30 |
| Proprietary Name | OXYCONTIN |
| Package Description | 30 TABLET in 1 BOTTLE (42549-645-30) |
| Product NDC | 42549-645 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | OXYCODONE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100808 |
| Marketing Category Name | NDA |
| Labeler Name | STAT Rx USA LLC |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
