NDC 70518-0743 – Ziprasidone Hydrochloride

Ziprasidone Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC70518-0743

Product details

Brand name
Ziprasidone Hydrochloride
Generic name
Ziprasidone Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA204375
Marketed since
September 20, 2017
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Ziprasidone hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
70518-0743-030 CAPSULE in 1 BLISTER PACK (70518-0743-0)Sep 20, 2017
70518-0743-130 POUCH in 1 BOX (70518-0743-1) / 1 CAPSULE in 1 POUCH (70518-0743-2)Aug 4, 2021
70518-0743-350 POUCH in 1 BOX (70518-0743-3) / 1 CAPSULE in 1 POUCH (70518-0743-2)Jul 8, 2026

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