Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate
Product Images NDC 70710-1189

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate (NDC 70710-1189). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Pharmaceuticals (usa) 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

Image (5b0a6856 94c3 4d11 A1d5 E7135ebe12f1 01)

FDA Label Image

5 mg 100 Count Bottle Label (5b0a6856 94c3 4d11 A1d5 E7135ebe12f1 02)

This is a description of a medication with the NDC 70710-1184-1. The medication is in the form of extended-release capsules and is a mixed salt of a single entity amphetamine product. It contains Dextroamphetamine Saccharate, Amphetamine Aspartate @ Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate. The medication is available in a bottle with 100 capsules and is for prescription use only. The pharmacist is advised to dispense the accompanying medication guide to each patient.*

FDA Label Image

10 mg 100 Count Bottle Label (5b0a6856 94c3 4d11 A1d5 E7135ebe12f1 03)

FDA Label Image

15 mg 100 Count Bottle Label (5b0a6856 94c3 4d11 A1d5 E7135ebe12f1 04)

This is a medication used in the treatment of attention deficit hyperactivity disorder (ADHD) called Dextroamphetamine Saccharat Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release Capsules. The medication is packaged as 100 capsules with the NDC (National Drug Code) identifier of 70710-1186-1. A pharmacist should dispense the medication guide alongside the treatment, and it should be administered with a prescription only (Rx Only).*

FDA Label Image

20 mg 100 Count Bottle Label (5b0a6856 94c3 4d11 A1d5 E7135ebe12f1 05)

This text is a description of a medication with the NDC code 70710-1187-1. It is a mixed salts of a single entity amphetamine product in the form of extended-release capsules. The medication contains Dextroamphetamine Saccharate, Amphetamine Aspartate C Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate. It comes in a 20 mg dose and there are 100 capsules per bottle. The medication is only available with a prescription.*

FDA Label Image

25 mg 100 Count Bottle Label (5b0a6856 94c3 4d11 A1d5 E7135ebe12f1 06)

This is a prescription medication with the NDC 70710-1188-1 used for treating Attention Deficit Hyperactivity Disorder (ADHD). It contains a mixture of Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate in the form of extended-release capsules. Each capsule contains 25mg of the active ingredients. The pharmacist is instructed to dispense the medication guide to each patient along with the 100 capsules.*

FDA Label Image

30 mg 100 Count Bottle Label (5b0a6856 94c3 4d11 A1d5 E7135ebe12f1 07)

This is a prescription medication labeled as NDC 707, containing a combination of Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate in extended-release capsules form. The capsule strength is 30 mg, and it comes in a bottle of 100 capsules. The pharmacist should provide a Medication Guide to each patient. The manufacturer of the medication is Zydus and it is only available by prescription (Rx Only).*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.