Atorvastatin Calcium

Product NDC
51655-614
11-digit product format
516550614
Labeler code
51655
Product ID
51655-614_30f9e52a-9799-4d3a-9392-d692c53d6047
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atorvastatin Calcium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Northwind Pharmaceuticals
Application
ANDA091624
Marketing category
ANDA
Marketing start
2015-08-25
Marketing end
0000-00-00
Substance
ATORVASTATIN CALCIUM TRIHYDRATE
Active strength
10 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
51655-614-522023-04-17C16284748780-19d75b9d0-d06c-f424-e053-dadaa90a57ce81a6bc42-8bc9-4fa4-b851-ce844090ddc2
51655-614-522020-01-31C16284748780-19d75b9d0-d06c-f424-e053-dadaa90a57ce81a6bc42-8bc9-4fa4-b851-ce844090ddc2