Rosuvastatin

Product NDC
70771-1483
11-digit product format
707711483
Labeler code
70771
Product ID
70771-1483_adfb8a09-06b0-466b-9782-2189364f09fd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rosuvastatin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Zydus Lifesciences Limited
Application
ANDA206513
Marketing category
ANDA
Marketing start
2020-01-16
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
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70771-1483-0707711483001000 TABLET, FILM COATED in 1 BOTTLE (70771-1483-0) 2020-01-160000-00-00NoNoCurrent
70771-1483-170771148301100 TABLET, FILM COATED in 1 BOTTLE (70771-1483-1) 2020-01-160000-00-00NoNoCurrent
70771-1483-27077114830210 BLISTER PACK in 1 CARTON (70771-1483-2) > 10 TABLET, FILM COATED in 1 BLISTER PACK10 blister pack2020-01-160000-00-00NoNoCurrent
70771-1483-37077114830330 TABLET, FILM COATED in 1 BOTTLE (70771-1483-3) 2020-01-160000-00-00NoNoCurrent
70771-1483-570771148305500 TABLET, FILM COATED in 1 BOTTLE (70771-1483-5) 2020-01-160000-00-00NoNoCurrent
70771-1483-97077114830990 TABLET, FILM COATED in 1 BOTTLE (70771-1483-9) 2020-01-160000-00-00NoNoCurrent