| NDC Code | 70860-778-02 |
|---|
| Package Description | 10 VIAL in 1 CARTON (70860-778-02) / 2 mL in 1 VIAL (70860-778-41) |
|---|
| Product NDC | 70860-778 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Prochlorperazine Edisylate |
|---|
| Non-Proprietary Name | Prochlorperazine Edisylate |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20181108 |
|---|
| End Marketing Date | 20240831 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040540 |
|---|
| Manufacturer | Athenex Pharmaceutical Division, LLC. |
|---|
| Substance Name | PROCHLORPERAZINE EDISYLATE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
|---|