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Oxycodone hydrochloride
Oxycodone hydrochloride - 47781-264-01 - (Oxycodone hydrochloride)
Drug Information of Oxycodone hydrochloride
| Product NDC: | 47781-264 |
| 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: | 47781-264 |
| Labeler Name: | Alvogen, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202116 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120112 |
Package Information of Oxycodone hydrochloride
| Package NDC: | 47781-264-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (47781-264-01) |
NDC Information of Oxycodone hydrochloride
| NDC Code | 47781-264-01 |
| Proprietary Name | Oxycodone hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE (47781-264-01) |
| Product NDC | 47781-264 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxycodone hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120112 |
| Marketing Category Name | ANDA |
| Labeler Name | Alvogen, Inc. |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
