Aripiprazole Tablet, Orally Disintegrating
Product Images NDC 76483-101

Product Visual Gallery

This gallery contains 20 technical images submitted to the FDA as part of the official labeling for Aripiprazole (NDC 76483-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Square Pharmaceuticals Limited, 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 Orally Disintegrating Tablets, Usp 10 mg; 30 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 01)

Label for Aripiprazole Orally Disintegrating Tablets USP, 10 mg, manufactured by Square Pharmaceuticals Ltd. The label indicates a package containing 30 tablets for oral use. It includes storage instructions, a warning about phenylalanine content, and a note for pharmacists to dispense the medication guide to each patient. The label also states the product is prescription only (Rx only).*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 10 mg; 60 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 02)

Label for Aripiprazole Orally Disintegrating Tablets, USP 10 mg, showing a white and red design. The label includes the NDC number 76483-100-01 and indicates a quantity of 60 tablets. Manufactured by Square Pharmaceuticals Ltd., located in Dhaka, Bangladesh. The label contains instructions for pharmacists to dispense the medication guide, storage conditions, and a warning to keep the drug out of reach of children.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 10 mg; 90 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 03)

Label for Aripiprazole orally disintegrating tablets USP, 10 mg strength, manufactured by Square Pharmaceuticals Ltd. The label indicates a package of 90 tablets for prescription use only, with storage instructions and a warning for phenylketonurics. The label includes directions for pharmacists to dispense the medication guide to each patient.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 10 mg; 120 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 04)

Label for Aripiprazole Orally Disintegrating Tablets, USP 10 mg by Square Pharmaceuticals Limited. The label indicates a package size of 120 tablets, prescription only, with storage instructions and a pharmacist dispensing note. Manufactured by Square Pharmaceuticals Ltd in Bangladesh.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 15 mg; 30 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 05)

Label for Aripiprazole Orally Disintegrating Tablets, USP 15 mg, manufactured by Square Pharmaceuticals Limited. The label indicates a package of 30 tablets with prescription-only status. It includes storage instructions, phenylketonurics warning, and pharmacist dispensing guidance. The label design features yellow and black text on a white background with an area designated for barcode and pharma code.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 15 mg; 60 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 06)

Label for Aripiprazole 15 mg Orally Disintegrating Tablets, USP, manufactured by Square Pharmaceuticals Limited. The label indicates 60 tablets per package for prescription use only, with storage instructions and warning for phenylketonurics. It also includes manufacturing details and a pharmacist notice to dispense the medication guide.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 15 mg; 90 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 07)

Label for Aripiprazole Orally Disintegrating Tablets, USP 15 mg. The label includes the NDC 76483-101-02 and indicates the product contains 90 tablets. It is manufactured by Square Pharmaceuticals Ltd., Dhaka, Bangladesh. The label includes storage instructions and a warning to keep out of reach of children.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 15 mg; 120 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 08)

Label for Aripiprazole Orally Disintegrating Tablets USP 15 mg from Square Pharmaceuticals Ltd. The label indicates 120 tablets per container with prescription only (Rx only) status. It includes dosing guidance, storage instructions, phenylalanine content warning, and manufacturing details from Dhaka, Bangladesh.*

FDA Label Image

20-30 (0f04eb47 6772 4910 Bb80 55ab7a2217e5 20)

This is a drug facts and labeling panel for Aripiprazole Orally Disintegrating Tablets USP, 20 mg strength. It provides dosage information, manufacturer details (Square Pharmaceuticals Ltd., Bangladesh), packaging size (30 tablets, Rx only), and storage instructions. It also includes a phenylketonurics warning for phenylalanine content and a pharmacist dispensing note.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 20 mg; 60 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 09)

Label for Aripiprazole Orally Disintegrating Tablets USP, 20 mg strength, manufactured by Square Pharmaceuticals Ltd. The label specifies 60 tablets per package, intended for oral administration. The label includes storage instructions, phenylketonurics warning, pharmacist dispensing guidance, and a caution to keep out of reach of children.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 20 mg; 90 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 10)

Aripiprazole 20 mg Orally Disintegrating Tablets packaging label from Square Pharmaceuticals Limited. The label states the product name, dosage strength (20 mg), form (orally disintegrating tablets), quantity (90 tablets), and prescription status (Rx only). It includes storage instructions and a warning to keep the medication out of children's reach. Manufacturer information and a barcode are also visible.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 20 mg; 120 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 11)

Label for Aripiprazole 20 mg orally disintegrating tablets, USP, manufactured by Square Pharmaceuticals Ltd. The label shows the NDC 76483-102-03 and indicates a package containing 120 tablets, Rx only. It includes storage instructions, phenylketonurics warning, and pharmacy dispensing guidance.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 30 mg; 30 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 12)

Label for Aripiprazole 30 mg Orally Disintegrating Tablets, USP, containing 30 tablets. The label includes the NDC 76483-103-00, manufacturer Square Pharmaceuticals Ltd., Dhaka Unit, Bangladesh, and storage instructions. It specifies dispensing guidance and phenylketonurics warning.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 30 mg; 60 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 13)

Label for Aripiprazole Orally Disintegrating Tablets USP, 30 mg strength. The label indicates 60 tablets per package, manufactured by Square Pharmaceuticals Ltd, Bangladesh. It includes dosing environment instructions and a notice to dispense the medication guide. The label also states the presence of phenylalanine and storage conditions.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 30 mg; 90 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 14)

Aripiprazole 30 mg Orally Disintegrating Tablets, USP label by Square Pharmaceuticals Limited. The label indicates an NDC of 76483-103-02 and a package size of 90 tablets. It includes a pharmacist note to dispense the medication guide with each patient. Storage instructions and phenylketonurics content information are also present on the label.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, Usp 30 mg; 120 Counts (0f04eb47 6772 4910 Bb80 55ab7a2217e5 15)

Aripiprazole 30 mg Orally Disintegrating Tablets USP label by Square Pharmaceuticals Limited. The label shows 120 tablets, prescription use only. It includes storage and dispensing instructions and highlights the presence of phenylalanine for phenylketonurics.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, 10 mg (30 Tablets In 1 Carton) (0f04eb47 6772 4910 Bb80 55ab7a2217e5 16)

Aripiprazole Orally Disintegrating Tablets USP 10 mg packaging label shows a red and white carton design with dosage strength prominently displayed in a red box. The label includes directions, phenylketonurics warning, storage instructions, and manufacturer Square Pharmaceuticals Limited details. The package contains 30 tablets (3 x 10 unit dose).*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, 15 mg (30 Tablets In 1 Carton) (0f04eb47 6772 4910 Bb80 55ab7a2217e5 17)

Packaging label for Aripiprazole Orally Disintegrating Tablets, USP 15 mg. The label indicates oral disintegrating tablets in 30 tablets per package (3 x 10 unit dose). Manufactured by Square Pharmaceuticals Limited. The design uses a white background with yellow accents and includes dosage strength and usage instructions.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets 20 mg (30 Tablets In 1 Carton) (0f04eb47 6772 4910 Bb80 55ab7a2217e5 18)

Flat packaging label for Aripiprazole Orally Disintegrating Tablets USP 20 mg by Square Pharmaceuticals Limited. The label includes dosage strength (20 mg), dosage form (orally disintegrating tablets), quantity (30 tablets, 3x10), directions for use, storage instructions, and manufacturer details. It also contains serialization space, barcode, and pharmacist dispensing instructions.*

FDA Label Image

Aripiprazole Orally Disintegrating Tablets, 30 mg (30 Tablets In 1 Carton) (0f04eb47 6772 4910 Bb80 55ab7a2217e5 19)

Packaging label for Aripiprazole Orally Disintegrating Tablets USP, 30 mg, by Square Pharmaceuticals Limited. The carton design includes dosage strength prominently on multiple panels along with directions and storage information. The package contains 30 tablets in unit-dose blister packs, with warnings to keep out of reach of children and pharmacist dispensing guidance. Manufacturer location in Dhaka, Bangladesh is noted.*

* 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.