FDA.reportPublic FDA data

Atorvastatin Calcium

Product NDC
68071-4506
11-digit product format
680714506
Labeler code
68071
Product ID
68071-4506_71c1e4d1-fb91-debe-e053-2995a90a82af
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atorvastatin Calcium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA205300
Marketing category
ANDA
Marketing start
2017-05-04
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
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-4506-32020-05-15C16284748780-19d75b9d0-bb51-f424-e053-dadaa90a57ce71c1e4d1-fb90-debe-e053-2995a90a82af
68071-4506-62020-05-15C16284748780-19d75b9d0-bb51-f424-e053-dadaa90a57ce71c1e4d1-fb90-debe-e053-2995a90a82af
68071-4506-32020-01-31C16284748780-19d75b9d0-bb51-f424-e053-dadaa90a57ce71c1e4d1-fb90-debe-e053-2995a90a82af
68071-4506-62020-01-31C16284748780-19d75b9d0-bb51-f424-e053-dadaa90a57ce71c1e4d1-fb90-debe-e053-2995a90a82af