Medications with Generic Name Beginning ‘L’

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L-Cysteine Hydrochloride

L-Cysteine Hydrochloride Injection USP is indicated for use only after dilution as an additive to Crystalline Amino Acid Injections to meet the intravenous amino acid nutritional requirements of infants receiving total parenteral nutrition…

American Regent, Inc.8 October 2011

L-Cysteine Hydrochloride

L-Cysteine Hydrochloride Injection USP is intended for use only after dilution as an additive to Crystalline Amino Acid Injections to meet the intravenous amino acid nutritional…

Sandoz Inc27 August 2018

Labetalol Hydrochloride (Labetalol)

Labetalol hydrochloride injection is indicated for control of blood pressure in severe hypertension. CONTRAINDICATIONS: Labetalol hydrochloride injection is contraindicated in bronchial asthma, overt cardiac failure, greater-than-firstdegree heart…

Mylan Institutional LLC1 March 2012

Labetalol

Labetalol hydrochloride tablets are indicated in the management of hypertension. Labetalol hydrochloride tablets may be used alone or in combination with other antihypertensive agents, especially thiazide and loop diuretics. CONTRAINDICATIONS:…

Sun Pharmaceutical Industries, Inc.12 November 2014

Labetalol

Labetalol hydrochloride tablets are indicated in the management of hypertension. Labetalol hydrochloride tablets may be used alone or in combination with other antihypertensive agents,…

Marlex Pharmaceuticals Inc6 April 2018

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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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