Topiramate Tablet, Film Coated
Product Images NDC 68084-342

Product Visual Gallery

This gallery contains 15 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 68084-342). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Ahp34201

Topiramate 100 mg film-coated oral tablet. The round white tablet is imprinted with 'ZD 16' on one side and is plain on the other. Manufactured by American Health Packaging.*

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Ahp34401

Topiramate 25 mg film-coated tablet, round, white, with imprint "ZD 14" on one side and a blank other side. The image includes a millimeter scale for size reference. Labeled by American Health Packaging.*

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Ahp34301

Topiramate 15 mg round, white, film-coated oral tablet with imprint "ZD 15" on one side and plain on the other side, shown with a millimeter scale for size reference.*

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Ahp34521

Topiramate 100 mg film-coated round white oral tablets, imprinted with 'ZD 13' on one side and blank on the other. Manufactured by American Health Packaging.*

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Structured Formula (Structure)

Chemical structure diagram of Topiramate, illustrating its molecular bonds and arrangement, as depicted in the image.*

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Figure 1 Kaplan-meier Estimates Of Cumulative Rates For Time To First Seizure In Study 1 (087c12f7 E830 4d20 E063 6294a90a570b 00)

A line chart showing cumulative rates for time to first seizure over 500 days comparing Topiramate 50 mg/day (solid line) and Topiramate 400 mg/day (dashed line) in two groups of patients (N=234 and N=236 respectively). The chart includes a p-value of 0.0002 indicating statistical significance between the two dosage groups.*

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Figure 2 Reduction In 4-week Migraine Headache Frequency (studies 11 And 12 For Adults And Adolescents) (Figure 2)

A bar chart comparing the change from baseline to double-blind phase in average monthly migraine period rate for Placebo, and Topiramate at doses of 50 mg/day, 100 mg/day, and 200 mg/day in two separate studies. The y-axis shows change values with error bars representing standard error. Statistical significance levels are indicated with asterisks below some bars.*

FDA Label Image

25 mg Topiramate Tablets Carton.jpg (25 mg Topiramate Tablets Carton)

Topiramate 25 mg film-coated tablets label showing 100 tablets in a 10 x 10 count. The label includes NDC number 68084-342-01, manufacturer American Health Packaging, and instructions for pharmacists to dispense with a medication guide. It also contains storage information and drug protection warnings.*

FDA Label Image

25 mg Topiramate Tablet Blister.jpg (25 mg Topiramate Tablet Blister)

Topiramate 25 mg film-coated tablet label from American Health Packaging. The label includes the drug name, dosage strength, tablet form, a barcode, lot number, expiration date placeholders, and manufacturer location in Columbus, Ohio. The format is repeated multiple times on the sheet.*

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50 mg Topiramate Tablets Carton.jpg (50 mg Topiramate Tablets Carton)

Topiramate 50 mg tablets, USP, film-coated oral tablets, labeled for 100 tablets (10 x 10) by American Health Packaging. The label includes NDC 68084-343-01, barcode, storage instructions, dosage information, and a QR code for medication guide and prescribing information. The label specifies "Rx Only" and includes pharmacist dispensing instructions.*

FDA Label Image

50 mg Topiramate Tablet Blister.jpg (50 mg Topiramate Tablet Blister)

Topiramate 50 mg film-coated tablet labels from American Health Packaging. The labels identify the product as Topiramate Tablet, USP 50 mg, with a barcode and spaces for batch lot number and expiration date. The manufacturer is listed as American Health Packaging, Columbus, Ohio.*

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100 mg Topiramate Tablets Carton.jpg (100 mg Topiramate Tablets Carton)

Topiramate 100 mg tablets, USP, oral dosage form, film-coated, in a package of 100 tablets (10 x 10) from American Health Packaging. The label includes the NDC 68084-344-01, instructions for pharmacists to dispense a Medication Guide, storage conditions, and a QR code for medication guide and prescribing information. The packaging is marked Rx only.*

FDA Label Image

100 mg Topiramate Tablet Blister.jpg (100 mg Topiramate Tablet Blister)

Topiramate 100 mg film-coated tablet label from American Health Packaging. The label shows the product name, dosage strength, and dosage form. It includes space for expiration date and lot number, a barcode, and the manufacturer's location in Columbus, Ohio.*

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200 mg Topiramate Tablets Carton.jpg (200 mg Topiramate Tablets Carton)

Topiramate 200 mg film-coated tablets in a 30-count package (3 strips of 10 tablets) labeled by American Health Packaging. The label includes dosage form as tablets, USP, and states prescription only. It provides storage instructions, pharmacist dispensing guidance, and manufacturer and distributor information with an NDC code 68084-345-21.*

FDA Label Image

200 mg Topiramate Tablet Blister.jpg (200 mg Topiramate Tablet Blister)

Topiramate 200 mg film-coated tablets packaging labels from American Health Packaging. Each label displays the product name, strength (200 mg), dosage form (tablet), a barcode, lot number, expiration date, and the labeler's information (American Health Packaging, Columbus, Ohio). Ten identical label sections are shown in two columns.*

* 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.