Ziprasidone

Product NDC
72578-125
11-digit product format
725780125
Labeler code
72578
Product ID
72578-125_e02b7585-27db-4f92-a018-4ed89374da48
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ziprasidone
Dosage form
CAPSULE
Route
ORAL
Labeler
Viona Pharmaceuticals Inc
Application
ANDA208988
Marketing category
ANDA
Marketing start
2020-09-15
Marketing end
0000-00-00
Substance
ZIPRASIDONE HYDROCHLORIDE
Active strength
20 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72578-125ZIPRASIDONE CAPSULE [VIONA PHARMACEUTICALS INC]5Legacy NDC20221225_8f78b278-a0b3-47ce-bbad-5dad7012896a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72578-125-0572578012505500 CAPSULE in 1 BOTTLE (72578-125-05) 500 capsule2020-09-150000-00-00NoNoCurrent
72578-125-167257801251660 CAPSULE in 1 BOTTLE (72578-125-16) 60 capsule2020-09-150000-00-00NoNoCurrent
72578-125-80725780125808 BLISTER PACK in 1 CARTON (72578-125-80) > 10 CAPSULE in 1 BLISTER PACK8 blister pack2020-09-150000-00-00NoNoCurrent