Desipramine Hydrochloride Tablet, Film Coated
Product Images NDC 45963-343

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Desipramine Hydrochloride (NDC 45963-343). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Actavis Pharma, Inc., 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

9d202fae-figure-01 (Image 1)

9d202fae-figure-01 (Image 1)
Chemical structure of Desipramine Hydrochloride showing the tricyclic ring system attached to a side chain containing nitrogen and a hydrochloride group.*
FDA Label Image

1 (Image 10)

1 (Image 10)
Label for Desipramine Hydrochloride Tablets USP, 50 mg film-coated tablets, supplied in a bottle of 100 tablets. The label includes directions to dispense the accompanying Medication Guide, storage instructions, and manufacturer/distributor information listing Epic Pharma, LLC and Actavis Pharma, Inc. The label features the Actavis logo and NDC 45963-343-02.*
FDA Label Image

1 (Image 11)

1 (Image 11)
Label for Desipramine Hydrochloride Tablets USP 75 mg film-coated tablets, manufactured by Epic Pharma, LLC and distributed by Actavis Pharma, Inc. The label indicates a package count of 100 tablets, with storage instructions and cautions to keep out of reach of children. The label also includes the NDC number 45963-344-02.*
FDA Label Image

1 (Image 12)

1 (Image 12)
Desipramine Hydrochloride Tablets USP 100 mg film-coated oral tablets label. The label shows 100 tablets, Rx only, manufactured by Epic Pharma, LLC and distributed by Actavis Pharma, Inc. Instructions include dispensing the accompanying medication guide, storage at controlled room temperature, and warnings to keep medication out of reach of children. The label includes an NDC barcode and dosage instructions.*
FDA Label Image

1 (Image 13)

1 (Image 13)
Desipramine Hydrochloride Tablets USP 150 mg film-coated tablets package label displaying drug name, strength, and quantity of 50 tablets. The label includes directions to dispense the accompanying Medication Guide, storage instructions, and manufacturer Epic Pharma, LLC with distributor Actavis Pharma, Inc. The label also features a barcode and a caution to keep medication out of reach of children.*
FDA Label Image

9d202fae-figure-02 (Image 2)

9d202fae-figure-02 (Image 2)
Desipramine Hydrochloride 10 mg film-coated tablets carton by Actavis Pharma, Inc. The white box features the product name, strength, and dosage form, with a visible quantity indication and manufacturer branding.*
FDA Label Image

9d202fae-figure-03 (Image 3)

9d202fae-figure-03 (Image 3)
Desipramine Hydrochloride film-coated tablets in multiple dosage strengths (10 mg, 25 mg, 50 mg, 75 mg, 100 mg, 150 mg) as shown on the carton. The product is labeled by Actavis Pharma, Inc., indicating oral administration for human prescription use.*
FDA Label Image

9d202fae-figure-04 (Image 4)

9d202fae-figure-04 (Image 4)
Desipramine Hydrochloride 25 mg film-coated tablets in a blister pack. The pack contains ten tablets arranged in two rows of five. Tablets are round and yellow. No additional labeling or text is visible on the package in the image.*
FDA Label Image

9d202fae-figure-05 (Image 5)

9d202fae-figure-05 (Image 5)
Desipramine Hydrochloride 50 mg film-coated tablets packaging label. The label shows the product name, strength (50 mg), dosage form (tablet, film-coated), and includes the Actavis Pharma, Inc. labeler information. The image also features a blister pack containing yellow oval tablets.*
FDA Label Image

9d202fae-figure-06 (Image 6)

9d202fae-figure-06 (Image 6)
Desipramine Hydrochloride 25 mg film-coated tablets, round and pale yellow, embossed with 'D' on one side and '25' on the other. The image shows front and back views of the tablet. Manufactured by Actavis Pharma, Inc.*
FDA Label Image

9d202fae-figure-07 (Image 7)

9d202fae-figure-07 (Image 7)
Desipramine Hydrochloride 10 mg film-coated tablets carton by Actavis Pharma, Inc. The white and orange box includes the product name, strength, dosage form, and labeler information clearly printed. The package design features a clean layout with orange and green accents.*
FDA Label Image

1 (Image 8)

1 (Image 8)
Label for Desipramine Hydrochloride Tablets USP, 10 mg strength, film-coated oral tablets. The label indicates packaging of 100 tablets for prescription use only. It includes storage instructions, manufacturer EpicPharma LLC, and distributor Actavis Pharma, Inc. The label also features the NDC 45963-341-02 and a barcode.*
FDA Label Image

1 (Image 9)

1 (Image 9)
Label for Desipramine Hydrochloride 25 mg tablets USP by Actavis Pharma, Inc. The label states it contains 100 film-coated oral tablets, Rx only. It includes dispensing instructions and storage conditions, with manufacturer listed as Epic Pharma, LLC, and distributor as Actavis Pharma, Inc. The label shows NDC 45963-342-02 and a barcode.*

* 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.