Chlorpromazine Hydrochloride 70710-1133-04

Package NDC

70710-1133-04

Manufacturer: Zydus Pharmaceuticals (usa) Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 27, 2020
Listing Expires: December 31, 2026
Application: ANDA213368

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Active Ingredients

Ingredient	Strength
Chlorpromazine Hydrochloride	200 mg/1

Drug Class

Phenothiazine [EPC]Phenothiazines [CS]

Selected Package

70710-1133-04Selected

10 BLISTER PACK in 1 CARTON (70710-1133-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1133-2)

Other packages for this product(1)

70710-1133-01

100 TABLET, FILM COATED in 1 BOTTLE (70710-1133-1)

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