Simvastatin

Product NDC
51079-456
11-digit product format
510790456
Labeler code
51079
Product ID
51079-456_9af1b4b7-abf7-2bc7-e053-2a95a90a6153
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Simvastatin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA076052
Marketing category
ANDA
Marketing start
2006-07-10
Marketing end
2020-05-31
Substance
SIMVASTATIN
Active strength
40 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51079-456-01EA - Each51079-456b3fe931a-0bdf-4c7f-9a0e-102595c194b512013-05-02
51079-456-20EA - Each51079-456e6a9d9c6-8ba4-456f-9af1-17420439bb1712013-05-02