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oxycodone hydrochloride
oxycodone hydrochloride - 58177-679-04 - (oxycodone hydrochloride)
Drug Information of oxycodone hydrochloride
| Product NDC: | 58177-679 |
| 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, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of oxycodone hydrochloride
| Product NDC: | 58177-679 |
| Labeler Name: | Ethex Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020553 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20090925 |
Package Information of oxycodone hydrochloride
| Package NDC: | 58177-679-04 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (58177-679-04) |
NDC Information of oxycodone hydrochloride
| NDC Code | 58177-679-04 |
| Proprietary Name | oxycodone hydrochloride |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (58177-679-04) |
| Product NDC | 58177-679 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxycodone hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090925 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Ethex Corporation |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
