Diltiazem Hydrochloride

Product NDC

55154-4787

11-digit product format

551544787

Labeler code

55154

Product ID

55154-4787_62b2779c-46f2-4ea2-a1d2-c089333a4066

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diltiazem Hydrochloride

Dosage form

CAPSULE, COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Cardinal Health

Application

ANDA074984

Marketing category

ANDA

Marketing start

2012-12-11

Marketing end

0000-00-00

Substance

DILTIAZEM HYDROCHLORIDE

Active strength

180 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record