Ziprasidone Hydrochloride

Product NDC

57297-332

11-digit product format

572970332

Labeler code

57297

Product ID

57297-332_105d5a2d-7f6a-439e-bc9c-3d81b3077e74

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ziprasidone Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

LUPIN LIMITED

Application

ANDA077560

Marketing category

ANDA

Marketing start

2012-03-02

Marketing end

0000-00-00

Substance

ZIPRASIDONE HYDROCHLORIDE

Active strength

40 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record