ISOSORBIDE MONONITRATE

Product NDC

70518-0214

11-digit product format

705180214

Labeler code

70518

Product ID

70518-0214_9f8c5466-a47b-0d9e-e053-2995a90a9d12

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

isosorbide mononitrate

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075395

Marketing category

ANDA

Marketing start

2017-02-10

Marketing end

0000-00-00

Substance

ISOSORBIDE MONONITRATE

Active strength

30 mg/1

Pharmacologic classes

Nitrate Vasodilator [EPC],Nitrates [CS],Vasodilation [PE]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record