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Oxycodone Hydrochloride and Acetaminophen
Oxycodone Hydrochloride and Acetaminophen - 0603-4997-32 - (oxycodone hydrochloride and acetaminophen)
Drug Information of Oxycodone Hydrochloride and Acetaminophen
| Product NDC: | 0603-4997 |
| Proprietary Name: | Oxycodone Hydrochloride and Acetaminophen |
| Non Proprietary Name: | oxycodone hydrochloride and acetaminophen |
| Active Ingredient(s): | 500; 5 mg/1; mg/1 & nbsp; oxycodone hydrochloride and acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxycodone Hydrochloride and Acetaminophen
| Product NDC: | 0603-4997 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040106 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960730 |
Package Information of Oxycodone Hydrochloride and Acetaminophen
| Package NDC: | 0603-4997-32 |
| Package Description: | 1000 CAPSULE in 1 BOTTLE, PLASTIC (0603-4997-32) |
NDC Information of Oxycodone Hydrochloride and Acetaminophen
| NDC Code | 0603-4997-32 |
| Proprietary Name | Oxycodone Hydrochloride and Acetaminophen |
| Package Description | 1000 CAPSULE in 1 BOTTLE, PLASTIC (0603-4997-32) |
| Product NDC | 0603-4997 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxycodone hydrochloride and acetaminophen |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19960730 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
| Strength Number | 500; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
