Rosuvastatin calcium

Product NDC
71335-1717
11-digit product format
713351717
Labeler code
71335
Product ID
71335-1717_bf7a66bf-807d-40b8-a2de-ff8dbe4a9c45
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rosuvastatin calcium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA079172
Marketing category
ANDA
Marketing start
2016-07-19
Marketing end
0000-00-00
Substance
ROSUVASTATIN CALCIUM
Active strength
10 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-1717-17133517170130 TABLET, FILM COATED in 1 BOTTLE (71335-1717-1) 2020-10-230000-00-00NoNoCurrent
71335-1717-27133517170290 TABLET, FILM COATED in 1 BOTTLE (71335-1717-2) 2020-10-230000-00-00NoNoCurrent
71335-1717-37133517170360 TABLET, FILM COATED in 1 BOTTLE (71335-1717-3) 2020-10-230000-00-00NoNoCurrent
71335-1717-471335171704120 TABLET, FILM COATED in 1 BOTTLE (71335-1717-4) 2021-12-290000-00-00NoNoCurrent
71335-1717-571335171705180 TABLET, FILM COATED in 1 BOTTLE (71335-1717-5) 2021-12-290000-00-00NoNoCurrent