| NDC Code | 0121-0653-04 |
|---|
| Package Description | 120 mL in 1 BOTTLE, DROPPER (0121-0653-04) |
|---|
| Product NDC | 0121-0653 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Fluphenazine Hydrochloride |
|---|
| Non-Proprietary Name | Fluphenazine Hydrochloride |
|---|
| Dosage Form | SOLUTION, CONCENTRATE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100901 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA074725 |
|---|
| Manufacturer | PAI Holdings, LLC dba PAI Pharma |
|---|
| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
|---|