| NDC Code | 68083-435-10 |
|---|
| Package Description | 10 VIAL in 1 CARTON (68083-435-10) / 2 mL in 1 VIAL (68083-435-01) |
|---|
| Product NDC | 68083-435 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Prochlorperazine Edisylate |
|---|
| Non-Proprietary Name | Prochlorperazine Edisylate |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20210922 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA214107 |
|---|
| Manufacturer | Gland Pharma Limited |
|---|
| Substance Name | PROCHLORPERAZINE EDISYLATE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
|---|