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Oxycodone Hydrochloride
Oxycodone Hydrochloride - 68462-347-37 - (Oxycodone Hydrochloride)
Drug Information of Oxycodone Hydrochloride
| Product NDC: | 68462-347 |
| Proprietary Name: | Oxycodone Hydrochloride |
| Non Proprietary Name: | Oxycodone Hydrochloride |
| Active Ingredient(s): | 100 mg/5mL & nbsp; Oxycodone Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxycodone Hydrochloride
| Product NDC: | 68462-347 |
| Labeler Name: | Glenmark Generics, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA200535 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20101220 |
Package Information of Oxycodone Hydrochloride
| Package NDC: | 68462-347-37 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (68462-347-37) > 30 mL in 1 BOTTLE, PLASTIC |
NDC Information of Oxycodone Hydrochloride
| NDC Code | 68462-347-37 |
| Proprietary Name | Oxycodone Hydrochloride |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (68462-347-37) > 30 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 68462-347 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxycodone Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20101220 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Glenmark Generics, Inc |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
