PRAVASTATIN SODIUM

Product NDC
0615-8620
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PRAVASTATIN SODIUM
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Application
ANDA076341
Marketing category
ANDA
Substance
PRAVASTATIN SODIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
0615-8620-0515 TABLET in 1 BLISTER PACK (0615-8620-05) 2026-02-13NoHistorical
0615-8620-3930 TABLET in 1 BLISTER PACK (0615-8620-39) 2026-02-13NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PRAVASTATIN SODIUMNCS HealthCare of KY, LLC dba Vangard Labs | Apotex Inc.2026-02-27HUMAN PRESCRIPTION DRUG LABEL1