Ziprasidone hydrochloride

Product NDC
64679-992
11-digit product format
646790992
Labeler code
64679
Product ID
64679-992_83bb92ad-8d72-4b8d-958a-ff4c97c9c2ba
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ziprasidone hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Wockhardt USA LLC.
Application
ANDA090348
Marketing category
ANDA
Marketing start
2012-09-01
Marketing end
0000-00-00
Substance
ZIPRASIDONE HYDROCHLORIDE
Active strength
40 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
64679-992-02EA - Each64679-99267ae302e-648f-417e-bd05-4123ec14855a12013-02-13
64679-992-04EA - Each64679-992acfa80c9-3322-4521-8ec2-4a655298adf212013-02-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
64679-992-016467909920130 CAPSULE in 1 BOTTLE (64679-992-01) 30 capsule2012-09-010000-00-00NoNoCurrent
64679-992-026467909920260 CAPSULE in 1 BOTTLE (64679-992-02) 60 capsule2012-09-010000-00-00NoNoCurrent
64679-992-0364679099203100 CAPSULE in 1 BOTTLE (64679-992-03) 100 capsule2012-09-010000-00-00NoNoCurrent
64679-992-0464679099204500 CAPSULE in 1 BOTTLE (64679-992-04) 500 capsule2012-09-010000-00-00NoNoCurrent
64679-992-066467909920610 BLISTER PACK in 1 CARTON (64679-992-06) > 8 CAPSULE in 1 BLISTER PACK10 blister pack2012-09-010000-00-00NoNoCurrent