Diltiazem Hydrochloride

Product NDC

35356-907

11-digit product format

353560907

Labeler code

35356

Product ID

35356-907_5d6da333-0ee2-4935-a165-6c7707c0d296

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diltiazem Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA074185

Marketing category

ANDA

Marketing start

1995-12-26

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