Verapamil Hydrochloride

Product NDC

0378-0772

11-digit product format

003780772

Labeler code

0378

Product ID

0378-0772_9b6e9cd5-92ea-415a-88c3-e6f01e9bc3e2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

verapamil hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Pharmaceuticals Inc.

Application

ANDA071483

Marketing category

ANDA

Marketing start

1989-02-15

Marketing end

2020-11-30

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

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record