Atorvastatin Calcium

Product NDC
55700-548
11-digit product format
557000548
Labeler code
55700
Product ID
55700-548_82a737e0-3918-4cc8-af04-edb29b35f759
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atorvastatin Calcium
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA091650
Marketing category
ANDA
Marketing start
2017-08-18
Marketing end
0000-00-00
Substance
ATORVASTATIN CALCIUM TRIHYDRATE
Active strength
20 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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-548-30EA - Each55700-5482b923510-f92c-4861-8333-93a1a61261fd12018-03-08
55700-548-90EA - Each55700-548f3cc4569-aaa9-4f8b-9f36-a23b502e0cbd12017-09-11