Chlorpromazine Hydrochloride 16714-0049-01

Package NDC

16714-0049-01

Manufacturer: Northstar Rx Llc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 11, 2020
Listing Expires: December 31, 2026
Application: ANDA213368

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Active Ingredients

Ingredient	Strength
Chlorpromazine Hydrochloride	50 mg/1

Drug Class

Phenothiazine [EPC]Phenothiazines [CS]

Selected Package

16714-0049-01Selected

100 TABLET, FILM COATED in 1 BOTTLE (16714-049-01)