Chlorpromazine Hydrochloride 65219-0130
Product NDC
65219-0130- Manufacturer
- Fresenius Kabi Usa, Llc
- Dosage Form
- Injection
- Route
- Intramuscular
- Product Type
- Human Prescription Drug
- Marketing Start
- February 15, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA216724
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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 (65219-130-02) / 2 mL in 1 VIAL (65219-130-01)