Isoniazid 300 Mg
Product Images NDC 83112-071

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Isoniazid 300 Mg (NDC 83112-071). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Health Department, Oklahoma State, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Isoniazid Card (1ebf0abe 1f5f 4731 Ab5c 2f3cc742db29)

Isoniazid Card (1ebf0abe 1f5f 4731 Ab5c 2f3cc742db29)
Packaging label for Isoniazid 300 mg tablets by Oklahoma State Department of Health. The label includes a 30-day SureMed by Omnicell medication calendar with numbered slots for daily doses. The label provides lot number, expiration date (12/15/2023), NDC, and manufacturer details (Teva). The calendar is designed for organized dispensing and storage instructions to keep the medication out of reach of children.*
FDA Label Image

Isoniazid Card Front (56d7a4d5 A91f 4b7e 922f 87e5e3f2c08b)

Isoniazid Card Front (56d7a4d5 A91f 4b7e 922f 87e5e3f2c08b)
Isoniazid 300 mg tablets in a 30-count blister card. The card is white with a yellow label at the top left indicating "ISONIAZID 300 MG TAB 30 COUNT." Tablets are arranged in rows with numbered days from 1 to 30 for dosing tracking. The labeler is Oklahoma State Health Department.*
FDA Label Image

F4378f13 6ee5 03f6 E053 2a95a90a206f

F4378f13 6ee5 03f6 E053 2a95a90a206f
Isoniazid 300 mg oblong white tablet with imprint 'b' on one side and '071 | 300' on the other. The tablet measures approximately 17 mm in length. Labeler is Health Department, Oklahoma State.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.