NDC 71335-1508 – Ziprasidone hydrochloride

Ziprasidone Hydrochloride 80 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1508

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, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
71335-1508-160 CAPSULE in 1 BOTTLE (71335-1508-1)May 2, 2019
71335-1508-230 CAPSULE in 1 BOTTLE (71335-1508-2)May 2, 2019
71335-1508-328 CAPSULE in 1 BOTTLE (71335-1508-3)May 2, 2019
71335-1508-490 CAPSULE in 1 BOTTLE (71335-1508-4)May 2, 2019

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