Diltiazem Hydrochloride

Product NDC

68071-3398

11-digit product format

680713398

Labeler code

68071

Product ID

68071-3398_5436a0ac-dd6a-4a34-e054-00144ff88e88

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

240 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