Chlorpromazine Hydrochloride 71656-0101-08

Package NDC

71656-0101-08

Manufacturer: Saptalis Pharmaceuticals, Llc.
Dosage Form: Concentrate
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 4, 2026
Listing Expires: December 31, 2027
Application: ANDA080983

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Active Ingredients

Ingredient	Strength
Chlorpromazine Hydrochloride	100 mg/mL

Drug Class

Phenothiazine [EPC]Phenothiazines [CS]

Selected Package

71656-0101-08Selected

240 mL in 1 BOTTLE, PLASTIC (71656-101-08)