Product NDC: | 16590-947 |
Proprietary Name: | ENDODAN |
Non Proprietary Name: | OXYCODONE and ASPIRIN |
Active Ingredient(s): | 325; 4.8355 mg/1; mg/1 & nbsp; OXYCODONE and ASPIRIN |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-947 |
Labeler Name: | STAT RX USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA007337 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 19940520 |
Package NDC: | 16590-947-60 |
Package Description: | 60 TABLET in 1 BOTTLE (16590-947-60) |
NDC Code | 16590-947-60 |
Proprietary Name | ENDODAN |
Package Description | 60 TABLET in 1 BOTTLE (16590-947-60) |
Product NDC | 16590-947 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | OXYCODONE and ASPIRIN |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19940520 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | STAT RX USA LLC |
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] |