Verapamil Hydrochloride

Product NDC

0615-7619

11-digit product format

006157619

Labeler code

0615

Product ID

0615-7619_4ca4589b-28bd-4f8d-b1e8-3a4ba4323253

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Verapamil Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA070994

Marketing category

ANDA

Marketing start

1986-10-01

Marketing end

0000-00-00

Substance

VERAPAMIL HYDROCHLORIDE

Active strength

120 mg/1

Pharmacologic classes

P-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record