NDC 71335-0501 – Ziprasidone Hydrochloride

Ziprasidone Hydrochloride 80 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0501

Product details

Brand name
Ziprasidone Hydrochloride
Generic name
Ziprasidone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA204375
Marketed since
February 18, 2017
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
71335-0501-160 CAPSULE in 1 BOTTLE (71335-0501-1)May 22, 2018
71335-0501-230 CAPSULE in 1 BOTTLE (71335-0501-2)Sep 5, 2019
71335-0501-328 CAPSULE in 1 BOTTLE (71335-0501-3)Jun 28, 2022
71335-0501-490 CAPSULE in 1 BOTTLE (71335-0501-4)Jun 28, 2022

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