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Oxycodone Hydrochloride
Oxycodone Hydrochloride - 68382-796-01 - (Oxycodone Hydrochloride)
Drug Information of Oxycodone Hydrochloride
| Product NDC: | 68382-796 |
| Proprietary Name: | Oxycodone Hydrochloride |
| Non Proprietary Name: | Oxycodone Hydrochloride |
| Active Ingredient(s): | 20 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: | 68382-796 |
| Labeler Name: | Zydus Pharmaceuticals (USA) Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077290 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121226 |
Package Information of Oxycodone Hydrochloride
| Package NDC: | 68382-796-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (68382-796-01) |
NDC Information of Oxycodone Hydrochloride
| NDC Code | 68382-796-01 |
| Proprietary Name | Oxycodone Hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE (68382-796-01) |
| Product NDC | 68382-796 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxycodone Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121226 |
| Marketing Category Name | ANDA |
| Labeler Name | Zydus Pharmaceuticals (USA) Inc. |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
