Mirtazapine Tablet, Film Coated
Product Images NDC 66993-607

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Mirtazapine (NDC 66993-607). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Prasco Laboratories, 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

Chemical Structure (Mirtazapine Tablets Usp 1)

Chemical Structure (Mirtazapine Tablets Usp 1)
Chemical structure diagram of Mirtazapine, showing its molecular ring system and methyl group.*
FDA Label Image

7.5 30 (Mirtazapine Tablets Usp 2)

7.5 30 (Mirtazapine Tablets Usp 2)
Mirtazapine Tablets, USP 7.5 mg film-coated tablets carton label from Prasco Laboratories. The label includes dosage strength, quantity of 30 tablets, and prescription only indication. Additional details include storage instructions, NDC 66993-606-30, barcode, and medication guide website URL www.prasco.com/medguide/mirtazapine.*
FDA Label Image

7.5 500 (Mirtazapine Tablets Usp 3)

7.5 500 (Mirtazapine Tablets Usp 3)
Mirtazapine Tablets USP 7.5 mg film-coated oral tablets by Prasco Laboratories. The label indicates 500 tablets in the package, with storage instructions between 20 to 25°C (68 to 77°F). The label includes dispensing information and barcode with NDC 66993-606-04. Produced by Hampton Laine and made in Malta.*
FDA Label Image

15 30 (Mirtazapine Tablets Usp 4)

15 30 (Mirtazapine Tablets Usp 4)
Label for Mirtazapine Tablets USP 15 mg by Prasco Laboratories. The film-coated oral tablets are in a package of 30. The label includes the NDC 66993-607-30, dosage and storage instructions, manufacturer details, and a QR code. It specifies 'Rx only' and directs pharmacists to a medication guide at prasco.com.*
FDA Label Image

15 500 (Mirtazapine Tablets Usp 5)

15 500 (Mirtazapine Tablets Usp 5)
Label for Mirtazapine Tablets, USP 15 mg film-coated tablets. The label shows the manufacturer as Prasco Laboratories and the distributor Hampton Laine. It includes tablet ingredients, storage instructions (20°C to 25°C), dispensing information, and a 500-tablet count. The label also features the NDC 66993-607-04 and a QR code.*
FDA Label Image

30 30 (Mirtazapine Tablets Usp 6)

30 30 (Mirtazapine Tablets Usp 6)
Mirtazapine Tablets, USP 30 mg film-coated tablets, in a package of 30 tablets. The label includes dosing information, storage instructions, and directs pharmacists to dispense with the medication guide. The product is labeled by Prasco Laboratories and includes an NDC code and barcode. Manufactured in Malta, the label specifies prescription use only.*
FDA Label Image

30 500 (Mirtazapine Tablets Usp 7)

30 500 (Mirtazapine Tablets Usp 7)
Mirtazapine Tablets, USP 30 mg film-coated tablets package label from Prasco Laboratories. The label includes dosage strength (30 mg), quantity (500 tablets), and storage instructions. It displays the NDC code 66993-608-04, a barcode, manufacturer information, and a QR code. The label advises pharmacists to dispense with a Medication Guide available online.*
FDA Label Image

45 30 (Mirtazapine Tablets Usp 8)

45 30 (Mirtazapine Tablets Usp 8)
Mirtazapine Tablets USP 45 mg film-coated oral tablets packaging label. The label specifies 30 tablets per container, manufactured by Prasco Laboratories. It includes storage instructions, a caution for pharmacists to dispense with Medication Guide, and features a barcode and NDC number 66993-609-30. The label also shows expiration and lot number areas and indicates the product is made in Malta.*
FDA Label Image

45 500 (Mirtazapine Tablets Usp 9)

45 500 (Mirtazapine Tablets Usp 9)
Mirtazapine Tablets, USP 45 mg film-coated tablets in a 500-count bottle. The label includes dosage information, storage instructions, and a website for the medication guide. Manufactured for Prasco Laboratories, the label features the NDC 66993-609-04 and states Rx only.*

* 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.