Chlorpromazine Hydrochloride 73043-0049
Product NDC
73043-0049- Manufacturer
- Devatis, Inc.
- Dosage Form
- Injection
- Route
- Intramuscular
- Product Type
- Human Prescription Drug
- Marketing Start
- November 1, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA218229
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Chlorpromazine Hydrochloride | 25 mg/mL |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(1)
25 AMPULE in 1 CARTON (73043-049-25) / 2 mL in 1 AMPULE (73043-049-01)