Simvastatin

Product NDC

63739-435

11-digit product format

637390435

Labeler code

63739

Product ID

63739-435_56ce5280-96f7-44ca-8701-4f2bcc19cedb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Simvastatin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA077837

Marketing category

ANDA

Marketing start

2006-12-20

Marketing end

0000-00-00

Substance

SIMVASTATIN

Active strength

5 mg/1

Pharmacologic classes

HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record