Product Images Bupropion Hydrochloride SR

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Product Label Images

The following 4 images provide visual information about the product associated with Bupropion Hydrochloride SR NDC 0591-3540 by Actavis Pharma, Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Chemical Structure - image 1

Chemical Structure - image 1

NDC 0591-3540-60 Twice-A-Day (After Initial Titration) BuPROPion HCl Extended-release Tablets, USP (SR) 100 mg* - image 2

NDC 0591-3540-60 Twice-A-Day (After Initial Titration) BuPROPion HCl Extended-release Tablets, USP (SR) 100 mg* - image 2

This is a medication guide for BuPROPion HCI Extended-Release Tablets, USP (SR) with NDC 0591-3540-60. The tablets contain 100mg of Bupropion hydrochioride and are meant for twice-a-day use after initial titration. The medication guide contains a warning not to use in combination with ZYBAN or any other medications containing bupropion hydrochloride. Each tablet is meant to be taken orally and pharmacist is advised to dispense the accompanying medication guide to each patient. The usual dosage should be taken as per the instructions on the package insert. The tablets should be stored at 20° o 25°C (68" to 77°F). The medication is manufactured by Teva Pharmaceuticals.*

NDC 0591-3541-60 Twice-A-Day (After Initial Titration) BuPROPion HCl Extended-release Tablets, USP (SR) 150 mg* - image 3

NDC 0591-3541-60 Twice-A-Day (After Initial Titration) BuPROPion HCl Extended-release Tablets, USP (SR) 150 mg* - image 3

This is a description of a medication called Bupropion HCI, which is an extended-release tablet usually taken twice per day. The tablets contain 150mg of Bupropion hydrochloride, a potent medication that should not be combined with ZYBAN or any other drug containing Bupropion hydrochloride. The packaging recommends storing the medication at 68°F to 77°F, and the accompanying medication guide must be given to each patient along with the tablets. Additionally, the tablets are manufactured by Teva Pharmaceuticals, and caution is given to keep them away from children. Finally, there's a serialization coding area on the packaging.*

NDC 0591-3542-60 Twice-A-Day (After Initial Titration) BuPROPion HCl Extended-release Tablets, USP (SR) 200 mg* - image 4

NDC 0591-3542-60 Twice-A-Day (After Initial Titration) BuPROPion HCl Extended-release Tablets, USP (SR) 200 mg* - image 4

This is a warning label for a medication with the NDC code 0591-3542-60. The medication is an extended-release version of Bupropion HCI, which comes in tablet form with each tablet containing 200mg of the active ingredient. It is intended to be taken twice a day, with dosage instructions provided in the package insert. Patients should not use this medication in combination with another medication that contains Bupropion HCI, such as ZYBAN. The medication guide should be dispensed to every patient, and the medication should be stored at controlled room temperature. The manufacturer of the medication is Teva Pharmaceuticals.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.