Product NDC: | 42549-643 |
Proprietary Name: | OXYCODONE HYDROCHLORIDE |
Non Proprietary Name: | OXYCODONE HYDROCHLORIDE |
Active Ingredient(s): | 15 mg/1 & nbsp; OXYCODONE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42549-643 |
Labeler Name: | STAT Rx USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077712 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070131 |
Package NDC: | 42549-643-30 |
Package Description: | 30 TABLET in 1 BOTTLE (42549-643-30) |
NDC Code | 42549-643-30 |
Proprietary Name | OXYCODONE HYDROCHLORIDE |
Package Description | 30 TABLET in 1 BOTTLE (42549-643-30) |
Product NDC | 42549-643 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | OXYCODONE HYDROCHLORIDE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20070131 |
Marketing Category Name | ANDA |
Labeler Name | STAT Rx USA LLC |
Substance Name | OXYCODONE HYDROCHLORIDE |
Strength Number | 15 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |