Atomoxetine Capsule
Product Images NDC 31722-719

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Atomoxetine (NDC 31722-719). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Pharmaceuticals, 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

100mg (100mg)

Label for Atomoxetine Capsules USP 100 mg, containing 30 capsules. The label includes the NDC number 31722-720-30 and states the product is prescription only. It provides storage instructions (20° to 25°C), a pharmacist notice to dispense the Medication Guide, a U.S. contact number, and manufacturing details by Annora Pharma Pvt. Ltd. for Camber Pharmaceuticals, Inc.*

FDA Label Image

10mg (10mg)

Label for Atomoxetine Capsules, USP 10 mg by Camber Pharmaceuticals, Inc. The label indicates the product contains 30 capsules and is for oral use. It includes storage instructions, a pharmacy dispensing notice, U.S. contact information, manufacturer details, and a barcode. The strength 10 mg is highlighted on the label.*

FDA Label Image

18mg (18mg)

Label for Atomoxetine Capsules, USP 18 mg oral capsules by Camber Pharmaceuticals, Inc. The package contains 30 capsules. The label includes storage instructions at 20° to 25°C, a warning not to use if the inner seal is broken, and pharmacist dispensing instructions. Manufacturer information lists Annora Pharma Pvt. Ltd. in India. A barcode and NDC 31722-715-30 are also visible.*

FDA Label Image

25mg (25mg)

This packaging label is for Atomoxetine Capsules, USP 25 mg by Camber Pharmaceuticals, Inc. It contains 30 capsules and is for oral use. The label includes storage instructions, a pharmacist dispensing note, the NDC number 31722-716-30, and manufacturing details indicating it is made by Annora Pharma Pvt. Ltd. in India. A barcode and contact information are also visible.*

FDA Label Image

40mg (40mg)

Label for Atomoxetine Capsules USP 40 mg by Camber Pharmaceuticals, Inc., showing 30 capsules per bottle. The label includes storage instructions, a warning not to use if the inner seal is broken, contact information, and manufacturing details involving Annora Pharma Pvt. Ltd. A barcode is also visible on the right side of the label.*

FDA Label Image

60mg (60mg)

Label for Atomoxetine Capsules, USP 60 mg oral capsules from Camber Pharmaceuticals, Inc. The label includes NDC 31722-718-30 and indicates a bottle count of 30 capsules. Usage instructions, storage conditions, pharmacist dispensing note, and manufacturer details in Piscataway, NJ and Sangareddy, India, are also shown along with a barcode.*

FDA Label Image

80mg (80mg)

Atomoxetine Capsules, USP 80 mg oral capsules label from Camber Pharmaceuticals, Inc. The label indicates a package containing 30 capsules. Storage instructions and pharmacist dispensing guidance are included. The product is manufactured by Camber Pharmaceuticals, Inc. and Annora Pharma Pvt. Ltd.*

FDA Label Image

Camber (Camber)

FDA Label Image

Figure (Figure)

Two line charts depicting mean weight percentile and mean height percentile over 36 months of treatment. The left chart shows mean weight percentile changes for 203 subjects, while the right chart shows mean height percentile changes for 155 subjects, both with error bars indicating variability across months of treatment.*

FDA Label Image

Structure (Structure)

Chemical structure of Atomoxetine hydrochloride showing the molecular arrangement including aromatic rings and functional groups.*

* 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.