Isoniazid

Product NDC

43063-709

11-digit product format

430630709

Labeler code

43063

Product ID

43063-709_80104f11-de19-efae-e053-2a91aa0a7dd9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Isoniazid

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, 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