NDC 70518-3674 – Chlorpromazine Hydrochloride

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

Human Prescription Drug

Product NDC70518-3674

Product details

Brand name
Chlorpromazine Hydrochloride
Generic name
Chlorpromazine Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA084113
Marketed since
March 6, 2023
Listing expires
December 31, 2027
Pharmacologic class
Phenothiazine

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
70518-3674-0100 POUCH in 1 BOX (70518-3674-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3674-1)Mar 6, 2023
70518-3674-230 TABLET, FILM COATED in 1 BLISTER PACK (70518-3674-2)Dec 4, 2023
70518-3674-3100 POUCH in 1 BOX (70518-3674-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-3674-4)Aug 14, 2026

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