NDC 70710-1131 – Chlorpromazine hydrochloride

Chlorpromazine Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 6 recalls

Product NDC70710-1131

Product details

Brand name
Chlorpromazine hydrochloride
Generic name
Chlorpromazine hydrochloride
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213368
Marketed since
January 27, 2020
Listing expires
December 31, 2026
Pharmacologic class
Phenothiazine

Active ingredients

Uses, dosage, side effects and warnings for Chlorpromazine Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
70710-1131-1100 TABLET, FILM COATED in 1 BOTTLE (70710-1131-1)Jan 27, 2020
70710-1131-410 BLISTER PACK in 1 CARTON (70710-1131-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1131-2)Jan 27, 2020

Recalls mentioning this NDC

Other Chlorpromazine Hydrochloride products