Simvastatin

Product NDC
71610-610
11-digit product format
716100610
Labeler code
71610
Product ID
71610-610_ed131a35-eda8-4cdb-a6f0-eae48ea1c59e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Simvastatin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA078034
Marketing category
ANDA
Marketing start
2015-12-17
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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
AGG2FN16EVSIMVASTATIN79902-63-9SIMVASTATIN

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71610-610-307161006103030 TABLET, FILM COATED in 1 BOTTLE (71610-610-30) 2023-03-20NoNoHistorical
71610-610-457161006104545 TABLET, FILM COATED in 1 BOTTLE (71610-610-45) 2021-10-25NoNoHistorical
71610-610-607161006106090 TABLET, FILM COATED in 1 BOTTLE (71610-610-60) 2023-03-20NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
SimvastatinAphena Pharma Solutions - Tennessee, LLC2023-03-20HUMAN PRESCRIPTION DRUG LABEL2