Rosuvastatin Calcium

Product NDC
0093-7573
11-digit product format
000937573
Labeler code
0093
Product ID
0093-7573_83cfa277-158e-466a-8fcf-703495f858f7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rosuvastatin Calcium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Teva Pharmaceuticals USA, Inc.
Application
ANDA079166
Marketing category
ANDA
Marketing start
2016-08-18
Marketing end
2019-10-31
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
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0093-7573-56EA - Each0093-757308791352-497f-4e86-b9ec-edb9ae24352b12016-09-02