NDC 65862-703 – Ziprasidone Hydrochloride

Ziprasidone Hydrochloride 40 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC65862-703

Product details

Brand name
Ziprasidone Hydrochloride
Generic name
Ziprasidone Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA204117
Marketed since
December 27, 2016
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
65862-703-6060 CAPSULE in 1 BOTTLE (65862-703-60)Dec 27, 2016
65862-703-808 BLISTER PACK in 1 CARTON (65862-703-80) / 10 CAPSULE in 1 BLISTER PACK (65862-703-10)Dec 27, 2016
65862-703-991000 CAPSULE in 1 BOTTLE (65862-703-99)Dec 27, 2016

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