NDC Code | 14789-700-02 |
Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (14789-700-02) / 2 mL in 1 VIAL, SINGLE-DOSE (14789-700-07) |
Product NDC | 14789-700 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Prochlorperazine Edisylate |
Non-Proprietary Name | Prochlorperazine Edisylate |
Dosage Form | INJECTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20190225 |
Marketing Category Name | ANDA |
Application Number | ANDA204860 |
Manufacturer | Nexus Pharmaceuticals LLC |
Substance Name | PROCHLORPERAZINE EDISYLATE |
Strength | 5 |
Strength Unit | mg/mL |
Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |