Chlorpromazine Hydrochloride 73043-0048-25

Package NDC

73043-0048-25

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]

Selected Package

73043-0048-25Selected

25 AMPULE in 1 CARTON (73043-048-25) / 1 mL in 1 AMPULE (73043-048-01)