Diltiazem Hydrochloride

Product NDC

50090-0802

11-digit product format

500900802

Labeler code

50090

Product ID

50090-0802_092ba250-0e16-4b45-a464-03f434b6ae21

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Diltiazem Hydrochloride

Dosage form

CAPSULE, COATED, EXTENDED RELEASE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA074984

Marketing category

ANDA

Marketing start

1999-12-20

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