Rosuvastatin

Product NDC
70771-1481
11-digit product format
707711481
Labeler code
70771
Product ID
70771-1481_493a5304-a54c-41db-80b8-b2f25f09d829
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rosuvastatin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Cadila Healthcare Limited
Application
ANDA206513
Marketing category
ANDA
Marketing start
2020-01-16
Marketing end
0000-00-00
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
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70771-1481-0707711481001000 TABLET, FILM COATED in 1 BOTTLE (70771-1481-0) 2020-01-160000-00-00NoNoCurrent
70771-1481-170771148101100 TABLET, FILM COATED in 1 BOTTLE (70771-1481-1) 2020-01-160000-00-00NoNoCurrent
70771-1481-27077114810210 BLISTER PACK in 1 CARTON (70771-1481-2) > 10 TABLET, FILM COATED in 1 BLISTER PACK10 blister pack2020-01-160000-00-00NoNoCurrent
70771-1481-37077114810330 TABLET, FILM COATED in 1 BOTTLE (70771-1481-3) 2020-01-160000-00-00NoNoCurrent
70771-1481-570771148105500 TABLET, FILM COATED in 1 BOTTLE (70771-1481-5) 2020-01-160000-00-00NoNoCurrent
70771-1481-97077114810990 TABLET, FILM COATED in 1 BOTTLE (70771-1481-9) 2020-01-160000-00-00NoNoCurrent