Atorvastatin Calcium

Product NDC
68071-4185
11-digit product format
680714185
Labeler code
68071
Product ID
68071-4185_6027cff7-dfd7-5e5f-e053-2a91aa0ab548
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
2017-04-26
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
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-4185-92020-06-10C16284748780-19d75b9d0-4222-f424-e053-dadaa90a57ce6027a972-d156-3b99-e053-2a91aa0af474
68071-4185-92020-01-31C16284748780-19d75b9d0-4222-f424-e053-dadaa90a57ce6027a972-d156-3b99-e053-2a91aa0af474