Rosuvastatin

Product NDC
68382-630
11-digit product format
683820630
Labeler code
68382
Product ID
68382-630_1264fa84-af3e-42fe-933c-4c6f62e9b9e3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rosuvastatin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Zydus Pharmaceuticals (USA) Inc.
Application
ANDA206513
Marketing category
ANDA
Marketing start
2020-01-16
Marketing end
0000-00-00
Substance
ROSUVASTATIN CALCIUM
Active strength
40 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
68382-630-0168382063001100 TABLET, FILM COATED in 1 BOTTLE (68382-630-01) 2020-01-160000-00-00NoNoCurrent
68382-630-0568382063005500 TABLET, FILM COATED in 1 BOTTLE (68382-630-05) 2020-01-160000-00-00NoNoCurrent
68382-630-066838206300630 TABLET, FILM COATED in 1 BOTTLE (68382-630-06) 2020-01-160000-00-00NoNoCurrent
68382-630-10683820630101000 TABLET, FILM COATED in 1 BOTTLE (68382-630-10) 2020-01-160000-00-00NoNoCurrent
68382-630-166838206301690 TABLET, FILM COATED in 1 BOTTLE (68382-630-16) 2020-01-160000-00-00NoNoCurrent
68382-630-776838206307710 BLISTER PACK in 1 CARTON (68382-630-77) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-630-30) 10 blister pack2020-01-160000-00-00NoNoCurrent