Lovastatin

Product NDC

43063-731

11-digit product format

430630731

Labeler code

43063

Product ID

43063-731_7c731c1e-f307-1fec-e053-2a91aa0a7537

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lovastatin

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA075991

Marketing category

ANDA

Marketing start

2002-11-25

Marketing end

0000-00-00

Substance

LOVASTATIN

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