Ziprasidone

Product NDC
70771-1180
11-digit product format
707711180
Labeler code
70771
Product ID
70771-1180_58405edd-2565-4bbb-80fa-5b3cb9ff6f4f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ziprasidone
Dosage form
CAPSULE
Route
ORAL
Labeler
Zydus Lifesciences Limited
Application
ANDA208988
Marketing category
ANDA
Marketing start
2017-12-28
Marketing end
0000-00-00
Substance
ZIPRASIDONE HYDROCHLORIDE
Active strength
80 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
70771-1180ZIPRASIDONE CAPSULE [ZYDUS LIFESCIENCES LIMITED]5Legacy NDC20231005_d607e3c2-62f5-4f4c-bbb3-423ac9478420.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70771-1180-570771118005500 CAPSULE in 1 BOTTLE (70771-1180-5) 500 capsule2017-12-280000-00-00NoNoCurrent
70771-1180-67077111800660 CAPSULE in 1 BOTTLE (70771-1180-6) 60 capsule2017-12-280000-00-00NoNoCurrent
70771-1180-8707711180088 BLISTER PACK in 1 CARTON (70771-1180-8) > 10 CAPSULE in 1 BLISTER PACK (70771-1180-2) 8 blister pack2017-12-280000-00-00NoNoCurrent