Diltiazem Hydrochloride

Product NDC

70518-1009

11-digit product format

705181009

Labeler code

70518

Product ID

70518-1009_8fe531d5-f31a-2909-e053-2a95a90ac716

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

diltiazem hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA020401

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2018-02-09

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

2020-12-31

Current FDA listing

Historical FDA.report record