NDC Code | 23155-294-41 |
Package Description | 25 VIAL in 1 PACKAGE (23155-294-41) / 2 mL in 1 VIAL (23155-294-31) |
Product NDC | 23155-294 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Prochlorperazine Edisylate |
Non-Proprietary Name | Prochlorperazine Edisylate |
Dosage Form | INJECTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20120326 |
Marketing Category Name | ANDA |
Application Number | ANDA204147 |
Manufacturer | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. |
Substance Name | PROCHLORPERAZINE EDISYLATE |
Strength | 5 |
Strength Unit | mg/mL |
Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |