Diltiazem Hydrochloride

Product NDC

68071-3290

11-digit product format

680713290

Labeler code

68071

Product ID

68071-3290_504b67f5-3103-4525-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diltiazem Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

NDA018602

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2010-12-25

Marketing end

0000-00-00

Substance

DILTIAZEM HYDROCHLORIDE

Active strength

60 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