Acitretin Capsule
Product Images NDC 0115-1751

8 FDA label images from Amneal Pharmaceuticals Of New York Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Acitretin (NDC 0115-1751). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Of New York Llc, 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

Causes Birth Defects (DO NOT GET PREGNANT)

Causes Birth Defects (DO NOT GET PREGNANT)
An illustration showing a silhouette of a pregnant woman inside a red prohibition circle with a diagonal slash. Text above and below the image warns that the product causes birth defects and advises not to get pregnant.*
FDA Label Image

Chemical Sructure Of Acitretin (Acitretin Capsules 2)

Chemical Sructure Of Acitretin (Acitretin Capsules 2)
Chemical structure of Acitretin showing a complex arrangement of carbon, hydrogen, and oxygen atoms including methyl groups and a carboxylic acid functional group.*
FDA Label Image

Do Not Get Pregnant Image (Acitretin Capsules 3)

Do Not Get Pregnant Image (Acitretin Capsules 3)
An illustrated warning sign depicting a silhouette of a pregnant woman inside a red circle with a diagonal line crossing it, accompanied by the text "CAUSES BIRTH DEFECTS" above and "DO NOT GET PREGNANT" below, emphasizing the risk of birth defects.*
FDA Label Image

Image-do Not Get Pregnant (Acitretin Capsules 4)

Image-do Not Get Pregnant (Acitretin Capsules 4)
An advisory illustration depicting a pregnant woman silhouette inside a red prohibition symbol. The text above reads 'CAUSES BIRTH DEFECTS' and below reads 'DO NOT GET PREGNANT,' indicating a warning about pregnancy risks associated with the medication Acitretin.*
FDA Label Image

Container Label 10 mg (Acitretin Capsules 5)

Container Label 10 mg (Acitretin Capsules 5)
Label for Acitretin Capsules USP 10 mg by Impax Generics. The label includes dosage strength, a pregnancy warning symbol, storage instructions at 20° to 25°C, manufacturer Micro-Sphere SA in Switzerland, and distributor Amneal Pharmaceuticals LLC in New Jersey. It also states to dispense the enclosed medication guide and indicates Rx only for 30 capsules.*
FDA Label Image

Container Label 17.5 (Acitretin Capsules 6)

Container Label 17.5 (Acitretin Capsules 6)
Acitretin Capsules USP 17.5 mg label from Impax Generics shows a 30-capsule bottle. The label includes dosage strength, storage instructions (20° to 25°C), and warnings about birth defects and light exposure. Manufacturer is Micro-Sphere SA, Switzerland; distributed by Amneal Pharmaceuticals LLC, NJ. Contains barcodes and a pink section with GTIN and lot details.*
FDA Label Image

Container Label 22.5 (Acitretin Capsules 7)

Container Label 22.5 (Acitretin Capsules 7)
Label for Acitretin Capsules, USP 22.5 mg by Impax Generics. The label lists the active ingredient Acitretin, 22.5 mg per capsule. It includes storage instructions, manufacturer Micro-Sphere SA in Switzerland, and distributor Amneal Pharmaceuticals LLC in New Jersey. The package contains 30 capsules and advises pharmacists to dispense the enclosed medication guide.*
FDA Label Image

Container Label 25 mg (Acitretin Capsules 8)

Container Label 25 mg (Acitretin Capsules 8)
Label for Acitretin Capsules, USP 25 mg, by Impax Generics. The label includes a warning about birth defects, storage instructions to keep at 20° to 25°C (68° to 77°F), and the requirement to dispense the enclosed Medication Guide. Manufactured by Micro-Sphere SA, Switzerland, and distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. The package contains 30 capsules.*

* 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.