ROSUVASTATIN CALCIUM

Product NDC
71205-355
11-digit product format
712050355
Labeler code
71205
Product ID
71205-355_0ddbf155-487b-4b05-b18b-f4d8b40c746e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ROSUVASTATIN CALCIUM
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA206434
Marketing category
ANDA
Marketing start
2016-10-31
Substance
ROSUVASTATIN CALCIUM
Active strength
5 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

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

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71205-355-307120503553030 TABLET, FILM COATED in 1 BOTTLE (71205-355-30) 2019-11-01NoNoHistorical
71205-355-607120503556060 TABLET, FILM COATED in 1 BOTTLE (71205-355-60) 2019-11-01NoNoHistorical
71205-355-907120503559090 TABLET, FILM COATED in 1 BOTTLE (71205-355-90) 2019-11-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ROSUVASTATIN CALCIUMProficient Rx LP2022-11-01HUMAN PRESCRIPTION DRUG LABEL2