Verapamil Hydrochloride

Product NDC

0093-3045

11-digit product format

000933045

Labeler code

0093

Product ID

0093-3045_dfa87de0-b5a5-45d8-af05-76bcb35e2123

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

verapamil hydrochloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Teva Pharmaceuticals USA Inc

Application

ANDA074587

Marketing category

ANDA

Marketing start

2014-04-07

Marketing end

2020-01-31

Substance

VERAPAMIL HYDROCHLORIDE

Active strength

240 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

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record