Product NDC: | 63481-121 |
Proprietary Name: | PERCODAN |
Non Proprietary Name: | oxycodone hydrochloride and aspirin |
Active Ingredient(s): | 325; 4.8355 mg/1; mg/1 & nbsp; oxycodone hydrochloride and aspirin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63481-121 |
Labeler Name: | Endo Pharmaceuticals Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA007337 |
Marketing Category: | NDA |
Start Marketing Date: | 19500412 |
Package NDC: | 63481-121-70 |
Package Description: | 100 TABLET in 1 BOTTLE (63481-121-70) |
NDC Code | 63481-121-70 |
Proprietary Name | PERCODAN |
Package Description | 100 TABLET in 1 BOTTLE (63481-121-70) |
Product NDC | 63481-121 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | oxycodone hydrochloride and aspirin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19500412 |
Marketing Category Name | NDA |
Labeler Name | Endo Pharmaceuticals Inc |
Substance Name | ASPIRIN; OXYCODONE HYDROCHLORIDE |
Strength Number | 325; 4.8355 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC],Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |