Diltiazem Hydrochloride

Product NDC

68071-3079

11-digit product format

680713079

Labeler code

68071

Product ID

68071-3079_4ab52a18-e552-14d9-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diltiazem Hydrochloride

Dosage form

CAPSULE, COATED, EXTENDED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record