Atomoxetine Hydrochloride Capsule
Product Images NDC 51407-100

9 FDA label images from Golden State Medical Supply, Inc. · 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 Atomoxetine Hydrochloride (NDC 51407-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

51407 100 30lb

51407 100 30lb
Label for Atomoxetine Hydrochloride oral capsules, USP, 10 mg strength. The package contains 30 capsules. Manufactured by Abotta Inc. and packaged by Golden State Medical Supply, Inc. The NDC number shown is 51407-100-30. The label includes storage instructions and a caution to see the package insert for dosage information. The product is marked Rx only.*
FDA Label Image

51407 101 30lb

51407 101 30lb
Label for Atomoxetine capsules, USP, 18 mg strength, in a package containing 30 capsules. The label includes the NDC number 51407-101-30 and indicates prescription use only (Rx only). Storage instructions specify controlled room temperature between 20° to 25°C, with permitted excursions. The labeler is Golden State Medical Supply, Inc.*
FDA Label Image

51407 102 30lb

51407 102 30lb
Label for Atomoxetine Hydrochloride capsules, USP 25 mg strength, in a bottle containing 30 capsules. The label includes the NDC number 51407-102-30 and states the product is for oral use. Storage conditions and a note to see the package insert for dosage information are also visible. The labeler is Golden State Medical Supply, Inc.*
FDA Label Image

51407 103 30lb

51407 103 30lb
Label for Atomoxetine Hydrochloride 40 mg capsules USP by Golden State Medical Supply, Inc. The label indicates a package of 30 capsules with NDC 51407-103-30 and provides storage instructions to maintain at controlled room temperature. The label includes a barcode, lot number, expiration date, and notes that it is an Rx only medication.*
FDA Label Image

51407 104 30lb

51407 104 30lb
Label for Atomoxetine Hydrochloride 60 mg capsules, USP, in a 30-capsule package. The label shows NDC 51407-104-30 and indicates the product is Rx only. Manufacturer is listed as GSMS Incorporated with production in Canada and packaging in Camarillo, CA, USA. The label includes storage instructions and a barcode.*
FDA Label Image

51407 105 30lb

51407 105 30lb
Label for Atomoxetine Hydrochloride capsules, USP, 80 mg strength. The package contains 30 capsules. The label includes the NDC number 51407-105-30 and states the product is Rx only. It also displays storage instructions and the labeler, Golden State Medical Supply, Inc.*
FDA Label Image

51407 106 30lb

51407 106 30lb
Label for Atomoxetine capsules, USP, 100 mg strength, in a 30-capsule package. The label displays the NDC number 51407-106-30 and indicates the product is prescription only. The capsules are manufactured by Golden State Medical Supply, Inc., with storage instructions for controlled room temperature.*
FDA Label Image

Atomfig1 (Atomfig1)

Atomfig1 (Atomfig1)
Two line graphs showing changes in mean weight percentile and mean height percentile over 36 months of treatment for atomoxetine hydrochloride. The left graph depicts mean weight percentile for 203 subjects, showing an initial decrease followed by a gradual increase. The right graph shows mean height percentile for 155 subjects, with generally stable values over time.*
FDA Label Image

Atomstructure (Atomstructure)

Atomstructure (Atomstructure)
Chemical structure of atomoxetine hydrochloride, showing its molecular arrangement with a methylphenyl group, an ether oxygen, and a hydrochloride salt indicated.*

* 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.