Abilify
Product Images NDC 21695-005

3 FDA label images from Rebel Distributors Corp. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Abilify (NDC 21695-005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp., 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

Aripiprazole Chemical Structure (217e52b5 3a7b 4bbe Af3c B18de7d426c3 01)

Aripiprazole Chemical Structure (217e52b5 3a7b 4bbe Af3c B18de7d426c3 01)
Chemical structure of aripiprazole, the active ingredient in ABILIFY. The diagram shows the molecular framework including two chlorine atoms attached to a benzene ring, a piperazine ring, and a quinolinone moiety connected by an ether linkage.*
FDA Label Image

Abilify 5mg Label (217e52b5 3a7b 4bbe Af3c B18de7d426c3 02)

Abilify 5mg Label (217e52b5 3a7b 4bbe Af3c B18de7d426c3 02)
Label for Abilify 5 mg tablets, package of 15. Each tablet contains 5 mg of Aripiprazole. The label includes NDC 21695-002-15 and states the product ID PA000215. The manufacturer is Bristol-Myers Squibb Company, Princeton, NJ. Packaged by Physician Partner, Thousand Oaks, CA, with storage instructions for controlled room temperature 15°-30°C (59°-86°F). The label emphasizes RX Only status.*
FDA Label Image

Abilify 10mg Label (217e52b5 3a7b 4bbe Af3c B18de7d426c3 03)

Abilify 10mg Label (217e52b5 3a7b 4bbe Af3c B18de7d426c3 03)
Label for Abilify 10 mg tablets, a supply of 30 tablets distributed by Physician Partner. Each tablet contains 10 mg of aripiprazole. The product ID is RA000330, manufactured by Bristol-Myers Squibb Company, Princeton, NJ. The label includes storage instructions to keep at controlled room temperature (15°-30°C) and to keep medication out of children's reach. The NDC is 21695-003-30.*

* 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.