Diltiazem Hydrochloride

Product NDC

15338-434

11-digit product format

153380434

Labeler code

15338

Product ID

15338-434_6815a490-0925-53e8-e053-2a91aa0ae212

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diltiazem Hydrochloride

Dosage form

CAPSULE, COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Apace Packaging, LLC

Application

ANDA074984

Marketing category

ANDA

Marketing start

2016-08-18

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

2019-12-31

Current FDA listing

Historical FDA.report record