Diltiazem Hydrochloride

Product NDC

68071-3199

11-digit product format

680713199

Labeler code

68071

Product ID

68071-3199_4b7c6d1c-1e73-59ac-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

diltiazem hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

NDA020401

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-08-20

Marketing end

0000-00-00

Substance

DILTIAZEM HYDROCHLORIDE

Active strength

120 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