Diltiazem Hydrochloride

Product NDC

0615-1342

11-digit product format

006151342

Labeler code

0615

Product ID

0615-1342_c5453821-e9e9-4ae2-a3e1-9d1b51b420b5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diltiazem Hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA074984

Marketing category

ANDA

Marketing start

1999-12-20

Marketing end

0000-00-00

Substance

DILTIAZEM HYDROCHLORIDE

Active strength

240 mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record