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Oxycodone Hydrochloride
Oxycodone Hydrochloride - 0527-1426-35 - (Oxycodone Hydrochloride)
Drug Information of Oxycodone Hydrochloride
| Product NDC: | 0527-1426 |
| Proprietary Name: | Oxycodone Hydrochloride |
| Non Proprietary Name: | Oxycodone Hydrochloride |
| Active Ingredient(s): | 20 mg/mL & nbsp; Oxycodone Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxycodone Hydrochloride
| Product NDC: | 0527-1426 |
| Labeler Name: | Lannett Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20060101 |
Package Information of Oxycodone Hydrochloride
| Package NDC: | 0527-1426-35 |
| Package Description: | 1 BOTTLE in 1 CARTON (0527-1426-35) > 15 mL in 1 BOTTLE |
NDC Information of Oxycodone Hydrochloride
| NDC Code | 0527-1426-35 |
| Proprietary Name | Oxycodone Hydrochloride |
| Package Description | 1 BOTTLE in 1 CARTON (0527-1426-35) > 15 mL in 1 BOTTLE |
| Product NDC | 0527-1426 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxycodone Hydrochloride |
| Dosage Form Name | SOLUTION, CONCENTRATE |
| Route Name | ORAL |
| Start Marketing Date | 20060101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Lannett Company, Inc. |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
