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Oxycodone Hydrochloride
Oxycodone Hydrochloride - 66689-401-50 - (Oxycodone Hydrochloride)
Drug Information of Oxycodone Hydrochloride
| Product NDC: | 66689-401 |
| Proprietary Name: | Oxycodone Hydrochloride |
| Non Proprietary Name: | Oxycodone Hydrochloride |
| Active Ingredient(s): | 5 mg/5mL & nbsp; Oxycodone Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxycodone Hydrochloride
| Product NDC: | 66689-401 |
| Labeler Name: | VistaPharm Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA201194 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120315 |
Package Information of Oxycodone Hydrochloride
| Package NDC: | 66689-401-50 |
| Package Description: | 5 TRAY in 1 CASE (66689-401-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (66689-401-01) (66689-401-01) |
NDC Information of Oxycodone Hydrochloride
| NDC Code | 66689-401-50 |
| Proprietary Name | Oxycodone Hydrochloride |
| Package Description | 5 TRAY in 1 CASE (66689-401-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (66689-401-01) (66689-401-01) |
| Product NDC | 66689-401 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxycodone Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20120315 |
| Marketing Category Name | NDA |
| Labeler Name | VistaPharm Inc. |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
