NDC 70518-4295 – Chlorpromazine Hydrochloride

Chlorpromazine Hydrochloride 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-4295

Product details

Brand name
Chlorpromazine Hydrochloride
Generic name
Chlorpromazine Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA084115
Marketed since
February 26, 2025
Listing expires
December 31, 2027
Pharmacologic class
Phenothiazine

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
70518-4295-0100 POUCH in 1 BOX (70518-4295-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4295-1)Feb 26, 2025
70518-4295-2100 POUCH in 1 BOX (70518-4295-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-4295-3)Sep 1, 2026

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