Atorvastatin Calcium

Product NDC
50090-1265
11-digit product format
500901265
Labeler code
50090
Product ID
50090-1265_e8b77d0a-ea2f-4cfe-8552-a51572054999
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atorvastatin Calcium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA091624
Marketing category
ANDA
Marketing start
2013-04-05
Marketing end
0000-00-00
Substance
ATORVASTATIN CALCIUM TRIHYDRATE
Active strength
80 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-1265-0EA - Each50090-126515ed3731-1d40-41df-b6f9-daa4896656bc12018-11-06
50090-1265-1EA - Each50090-12653914c32a-7562-4d47-b41a-94e466b6728e12018-11-06