Ziprasidone Hydrochloride

Product NDC

61786-867

11-digit product format

617860867

Labeler code

61786

Product ID

61786-867_3b6485c1-8a59-616d-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ziprasidone Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077565

Marketing category

ANDA

Marketing start

2016-08-31

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