Ranolazine

Product NDC

60687-460

11-digit product format

606870460

Labeler code

60687

Product ID

60687-460_9a266f39-716a-69f5-e053-2a95a90a91fc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranolazine

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

American Health Packaging

Application

ANDA201046

Marketing category

ANDA

Marketing start

2019-12-16

Marketing end

0000-00-00

Substance

RANOLAZINE

Active strength

500 mg/1

Pharmacologic classes

Anti-anginal [EPC],Cytochrome P450 3A Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA],Organic Cation Transporter 2 Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record