Chlorpromazine Hydrochloride 70710-1850
Product NDC
70710-1850- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Injection
- Route
- Intramuscular
- Product Type
- Human Prescription Drug
- Marketing Start
- March 29, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA217275
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Chlorpromazine Hydrochloride | 25 mg/mL |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(1)
25 VIAL in 1 CARTON (70710-1850-7) / 2 mL in 1 VIAL (70710-1850-1)