| NDC Code | 50474-150-49 |
|---|
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (50474-150-49) > 115 mL in 1 BOTTLE, PLASTIC |
|---|
| Product NDC | 50474-150 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Tussionex Pennkinetic |
|---|
| Non-Proprietary Name | Hydrocodone And Chlorpheniramine |
|---|
| Dosage Form | SUSPENSION, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19871231 |
|---|
| End Marketing Date | 20190630 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA019111 |
|---|
| Manufacturer | UCB Inc. |
|---|
| Substance Name | HYDROCODONE; CHLORPHENIRAMINE |
|---|
| Strength | 10; 8 |
|---|
| Strength Unit | mg/5mL; mg/5mL |
|---|
| Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
|---|
| DEA Schedule | CII |
|---|