Isoniazid

Product NDC

0185-4351

11-digit product format

001854351

Labeler code

0185

Product ID

0185-4351_df6953a0-9aaa-422f-8e82-df79845ba24e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Isoniazid

Dosage form

TABLET

Route

ORAL

Labeler

Eon Labs, Inc.

Application

NDA008678

Marketing category

NDA

Marketing start

1978-12-11

Marketing end

2020-06-30

Substance

ISONIAZID

Active strength

100 mg/1

Pharmacologic classes

Antimycobacterial [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record