Rosuvastatin calcium

Product NDC
68788-8368
11-digit product format
687888368
Labeler code
68788
Product ID
68788-8368_90b0a5b7-3559-4c11-b760-b694e73b51a7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rosuvastatin calcium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.,
Application
ANDA079172
Marketing category
ANDA
Marketing start
2023-02-01
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
68788-8368-36878883680330 TABLET, FILM COATED in 1 BOTTLE (68788-8368-3) 2023-02-01NoNoHistorical
68788-8368-66878883680660 TABLET, FILM COATED in 1 BOTTLE (68788-8368-6) 2023-02-01NoNoHistorical
68788-8368-96878883680990 TABLET, FILM COATED in 1 BOTTLE (68788-8368-9) 2023-02-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Rosuvastatin calciumPreferred Pharmaceuticals Inc.,2025-09-18HUMAN PRESCRIPTION DRUG LABEL4