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Oxycodone Hydrochloride
Oxycodone Hydrochloride - 0603-4991-32 - (Oxycodone Hydrochloride)
Drug Information of Oxycodone Hydrochloride
| Product NDC: | 0603-4991 |
| 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) |
Labeler Information of Oxycodone Hydrochloride
| Product NDC: | 0603-4991 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077712 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070131 |
Package Information of Oxycodone Hydrochloride
| Package NDC: | 0603-4991-32 |
| Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-4991-32) |
NDC Information of Oxycodone Hydrochloride
| NDC Code | 0603-4991-32 |
| Proprietary Name | Oxycodone Hydrochloride |
| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-4991-32) |
| Product NDC | 0603-4991 |
| 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 | Qualitest Pharmaceuticals |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
