NDC 60687-441 – Chlorpromazine Hydrochloride

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

Human Prescription Drug 4 recalls

Product NDC60687-441

Product details

Brand name
Chlorpromazine Hydrochloride
Generic name
Chlorpromazine Hydrochloride
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209755
Marketed since
May 16, 2019
Listing expires
December 31, 2026
Pharmacologic class
Phenothiazine

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
60687-441-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-441-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-441-11)May 16, 2019

Recalls mentioning this NDC

Other Chlorpromazine Hydrochloride products