Prochlorperazine Edisylate 68083-0435
Product NDC
68083-0435- Manufacturer
- Gland Pharma Limited
- Dosage Form
- Injection
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- September 22, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA214107
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Prochlorperazine Edisylate | 5 mg/mL |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(2)
10 VIAL in 1 CARTON (68083-435-10) / 2 mL in 1 VIAL (68083-435-01)
25 VIAL in 1 CARTON (68083-435-25) / 2 mL in 1 VIAL (68083-435-01)