Isoniazid

Product NDC

60687-158

11-digit product format

606870158

Labeler code

60687

Product ID

60687-158_8647bdca-c02a-2b5f-e053-2a91aa0ac243

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Isoniazid

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

ANDA089776

Marketing category

ANDA

Marketing start

2016-02-23

Marketing end

2020-01-31

Substance

ISONIAZID

Active strength

300 mg/1

Pharmacologic classes

Antimycobacterial [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record