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ENDOCET
ENDOCET - 60951-700-70 - (Oxycodone and Acetaminophen)
Drug Information of ENDOCET
| Product NDC: | 60951-700 |
| Proprietary Name: | ENDOCET |
| Non Proprietary Name: | Oxycodone and Acetaminophen |
| Active Ingredient(s): | 325; 7.5 mg/1; mg/1 & nbsp; Oxycodone and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ENDOCET
| Product NDC: | 60951-700 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040434 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030306 |
Package Information of ENDOCET
| Package NDC: | 60951-700-70 |
| Package Description: | 100 TABLET in 1 BOTTLE (60951-700-70) |
NDC Information of ENDOCET
| NDC Code | 60951-700-70 |
| Proprietary Name | ENDOCET |
| Package Description | 100 TABLET in 1 BOTTLE (60951-700-70) |
| Product NDC | 60951-700 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxycodone and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030306 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
| Strength Number | 325; 7.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
