Medication Brand Names Beginning with ‘D’

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D-Care 100X (Lidocaine Hydrochloride, Povidone-Iodine, Isopropyl Alcohol)

Xylocaine (lidocaine HCl) Injections are indicated for production of local or regional anesthesia by infiltration techniques such as percutaneous injection and intravenous regional…

RX PHARMA-PACK, INC.31 January 2020

D-Penamine (Penicillamine)

Dear Health Care Provider: Due to the shortage of penicillamine titratable tablets in the United States (U.S.) market. Mylan is coordinating with the U.S. Food and Drug Administration…

Mylan Pharmaceuticals Inc.13 November 2018

D.H.E. 45 (Dihydroergotamine Mesylate)

D.H.E. 45 (dihydroergotamine mesylate) Injection USP is indicated for the acute treatment of migraine headaches with or without aura and the acute treatment of cluster headache episodes…

Valeant Pharmaceuticals North America6 November 2017

D.H.E. 45 (Dihydroergotamine Mesylate)

D.H.E. 45 (dihydroergotamine mesylate) Injection USP is indicated for the acute treatment of migraine headaches with or without aura and the acute treatment of cluster headache episodes…

Bausch Health US, LLC1 November 2019

Dabigatran Etexilate

Dabigatran Etexilate Capsules is a direct thrombin inhibitor indicated: To reduce the risk of stroke and systemic embolism in patients with non-valvular atrial fibrillation (1.1) For the…

Ascend Laboratories, LLC12 March 2020

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FDA Medwatch

Fusion Health and Vitality Issues Voluntary Nationwide Recall of Core Essential Nutrients and Immune Boost Sublingual Vitamin D3 Due to the Unapproved Use of a Food Additive and Unapproved Marketing Statements
Sun, 22 Nov 2020. Fusion Health and Vitality LLC is voluntarily recalling all 2020 Lots of CORE essential nutrients and Immune Boost Sublingual Vitamin D3. CORE has been found to contain an unapproved food additive, hordenine HCl, rendering it adulterated. Immune…
Fresenius Kabi Issues Voluntary Nationwide Recall of a Single Lot of Dexmedetomidine Hydrochloride Injection Due to Cross-Contamination of Lidocaine
Wed, 18 Nov 2020. Fresenius Kabi USA is voluntarily recalling a single lot of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg/50 mL (4 mcg /mL), 50 mL fill in a 50 mL vial. Fresenius Kabi initiated this recall due to a trace amount of lidocaine present…

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