| NDC Code | 17856-0079-5 |
|---|
| Package Description | 5 mL in 1 CUP (17856-0079-5) |
|---|
| Product NDC | 17856-0079 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Acetaminophen And Codeine Phosphate |
|---|
| Non-Proprietary Name | Acetaminophen And Codeine Phosphate |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19960426 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040119 |
|---|
| Manufacturer | ATLANTIC BIOLOGICALS COPR. |
|---|
| Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
|---|
| Strength | 120; 12 |
|---|
| Strength Unit | mg/5mL; mg/5mL |
|---|
| Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
|---|
| DEA Schedule | CV |
|---|