Rosuvastatin Calcium

Product NDC
50090-3549
11-digit product format
500903549
Labeler code
50090
Product ID
50090-3549_4697fc2b-734e-4194-8f4d-a136ff287bcb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rosuvastatin Calcium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA079172
Marketing category
ANDA
Marketing start
2016-07-19
Marketing end
0000-00-00
Substance
ROSUVASTATIN CALCIUM
Active strength
20 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
83MVU38M7QROSUVASTATIN CALCIUM147098-20-2ROSUVASTATIN CALCIUM

Packages

Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-3549-05009035490030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3549-0) 2016-07-190000-00-00NoNoCurrent
50090-3549-15009035490190 TABLET, FILM COATED in 1 BOTTLE (50090-3549-1) 2018-08-230000-00-00NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Rosuvastatin CalciumA-S Medication Solutions2019-04-29HUMAN PRESCRIPTION DRUG LABEL5