NDC 71335-2236 – Ziprasidone hydrochloride

Ziprasidone Hydrochloride 40 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2236

Product details

Brand name
Ziprasidone hydrochloride
Generic name
Ziprasidone hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077565
Marketed since
March 2, 2012
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
71335-2236-160 CAPSULE in 1 BOTTLE (71335-2236-1)Sep 7, 2023
71335-2236-228 CAPSULE in 1 BOTTLE (71335-2236-2)Sep 7, 2023
71335-2236-330 CAPSULE in 1 BOTTLE (71335-2236-3)Sep 7, 2023
71335-2236-490 CAPSULE in 1 BOTTLE (71335-2236-4)Sep 7, 2023

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