Lovastatin

Product NDC

50090-2278

11-digit product format

500902278

Labeler code

50090

Product ID

50090-2278_8e3a7d24-1a7e-4c6e-89f6-b8195b4fc86c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lovastatin

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA075636

Marketing category

ANDA

Marketing start

2001-12-17

Marketing end

0000-00-00

Substance

LOVASTATIN

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