Diltiazem Hydrochloride

Product NDC

70518-0783

11-digit product format

705180783

Labeler code

70518

Product ID

70518-0783_8e677efe-5c0b-26ec-e053-2995a90aba52

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diltiazem Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA018602

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2017-10-11

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

2020-12-31

Current FDA listing

Historical FDA.report record