NDC 70518-1835 – Ziprasidone hydrochloride

Ziprasidone Hydrochloride 20 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC70518-1835

Product details

Brand name
Ziprasidone hydrochloride
Generic name
Ziprasidone hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077565
Marketed since
January 30, 2019
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
70518-1835-030 CAPSULE in 1 BLISTER PACK (70518-1835-0)Jan 30, 2019

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