NDC Code | 0615-7792-39 |
Package Description | 30 TABLET in 1 BLISTER PACK (0615-7792-39) |
Product NDC | 0615-7792 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Acetaminophen And Codeine Phosphate |
Non-Proprietary Name | Acetaminophen And Codeine Phosphate |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 19900930 |
Marketing Category Name | ANDA |
Application Number | ANDA088628 |
Manufacturer | NCS HealthCare of KY, Inc dba Vangard Labs |
Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
Strength | 300; 30 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CIII |