diltiazem hydrochloride

Product NDC

70518-2071

11-digit product format

705182071

Labeler code

70518

Product ID

70518-2071_88df3768-55b4-8103-e053-2a95a90aa042

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

diltiazem hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA206534

Marketing category

ANDA

Marketing start

2019-05-10

Marketing end

0000-00-00

Substance

DILTIAZEM HYDROCHLORIDE

Active strength

180 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