NDC 16714-835 – Ziprasidone

Ziprasidone Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC16714-835

Product details

Brand name
Ziprasidone
Generic name
Ziprasidone
Labeler
NorthStar Rx LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077565
Marketed since
July 26, 2018
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Ziprasidone →

Package NDC codes (1)

Package NDCDescriptionSince
16714-835-0160 CAPSULE in 1 BOTTLE (16714-835-01)Jul 26, 2018

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