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Oxymorphone Hydrochloride
Oxymorphone Hydrochloride - 10702-070-01 - (Oxymorphone Hydrochloride)
Drug Information of Oxymorphone Hydrochloride
| Product NDC: | 10702-070 |
| 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: | 10702-070 |
| Labeler Name: | KVK-Tech, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA203601 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130211 |
Package Information of Oxymorphone Hydrochloride
| Package NDC: | 10702-070-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (10702-070-01) |
NDC Information of Oxymorphone Hydrochloride
| NDC Code | 10702-070-01 |
| Proprietary Name | Oxymorphone Hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE (10702-070-01) |
| Product NDC | 10702-070 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxymorphone Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130211 |
| Marketing Category Name | ANDA |
| Labeler Name | KVK-Tech, Inc. |
| Substance Name | OXYMORPHONE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
