Rosuvastatin Calcium

Product NDC
70518-2542
11-digit product format
705182542
Labeler code
70518
Product ID
70518-2542_c9fe9e67-cae9-5050-e053-2a95a90ae2c7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rosuvastatin Calcium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA208898
Marketing category
ANDA
Marketing start
2020-01-14
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
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-2542ROSUVASTATIN CALCIUM TABLET, FILM COATED [REMEDYREPACK INC.]10Legacy NDC20250321_ff96db35-2b35-4380-a28d-8048011eae5c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
70518-2542-07051825420030 TABLET, FILM COATED in 1 BLISTER PACK (70518-2542-0) 2020-01-140000-00-00NoNoCurrent
70518-2542-17051825420190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2542-1) 2021-03-180000-00-00NoNoCurrent