Rosuvastatin Calcium

Product NDC
69539-009
11-digit product format
695390009
Labeler code
69539
Product ID
69539-009_d60d5829-60cf-407c-8b23-45f010949311
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rosuvastatin Calcium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
MSN LABORATORIES PRIVATE LIMITED
Application
ANDA208898
Marketing category
ANDA
Marketing start
2017-11-22
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
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69539-009ROSUVASTATIN CALCIUM TABLET, FILM COATED [MSN LABORATORIES PRIVATE LIMITED]16Legacy NDC20250201_ec43549b-a0c6-4350-9568-8ebf1766303b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69539-009-0569539000905500 TABLET, FILM COATED in 1 BOTTLE (69539-009-05) 2019-02-250000-00-00NoNoCurrent
69539-009-0669539000906100 BLISTER PACK in 1 CARTON (69539-009-06) > 10 TABLET, FILM COATED in 1 BLISTER PACK (69539-009-11) 100 blister pack2017-11-220000-00-00NoNoCurrent
69539-009-906953900099090 TABLET, FILM COATED in 1 BOTTLE (69539-009-90) 2017-11-220000-00-00NoNoCurrent
69539-009-99695390009991000 TABLET, FILM COATED in 1 BOTTLE (69539-009-99) 2017-11-220000-00-00NoNoCurrent