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OXYMORPHONE HYDROCHLORIDE
OXYMORPHONE HYDROCHLORIDE - 0406-1009-01 - (Oxymorphone Hydrochloride)
Drug Information of OXYMORPHONE HYDROCHLORIDE
| Product NDC: | 0406-1009 |
| Proprietary Name: | OXYMORPHONE HYDROCHLORIDE |
| Non Proprietary Name: | Oxymorphone Hydrochloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; Oxymorphone Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OXYMORPHONE HYDROCHLORIDE
| Product NDC: | 0406-1009 |
| Labeler Name: | Mallinckrodt, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202321 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120412 |
Package Information of OXYMORPHONE HYDROCHLORIDE
| Package NDC: | 0406-1009-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0406-1009-01) |
NDC Information of OXYMORPHONE HYDROCHLORIDE
| NDC Code | 0406-1009-01 |
| Proprietary Name | OXYMORPHONE HYDROCHLORIDE |
| Package Description | 100 TABLET in 1 BOTTLE (0406-1009-01) |
| Product NDC | 0406-1009 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxymorphone Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120412 |
| Marketing Category Name | ANDA |
| Labeler Name | Mallinckrodt, Inc. |
| Substance Name | OXYMORPHONE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
