Lake Erie Medical DBA Quality Care Products LLC Products: Prescription Medications Section

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Abilify (Aripiprazole)

1 INDICATIONS AND USAGE 1.1 Schizophrenia ABILIFY is indicated for the treatment of schizophrenia. The efficacy of ABILIFY was established in four 4-6 week trials in adults and one 6-week trial in adolescents (13 to 17 years). Maintenance efficacy…

Lake Erie Medical DBA Quality Care Products LLC3 June 2010

ACETAMINOPHEN AND CODEINE PHOSPHATE

Acetaminophen and codeine phosphate tablets are indicated for the relief of mild to moderately severe pain. CONTRAINDICATIONS: Codeine-containing products are contraindicated for…

Lake Erie Medical DBA Quality Care Products LLC8 October 2020

Acetic Acid

For the treatment of superficial infections of the external auditory canal caused by organisms susceptible to the action of the antimicrobial. CONTRAINDICATIONS: Hypersensitivity to…

Lake Erie Medical DBA Quality Care Products LLC19 May 2020

Acyclovir

Herpes Zoster Infections: Acyclovir tablets are indicated for the acute treatment of herpes zoster (shingles). Genital Herpes: Acyclovir tablets are indicated for the treatment of initial…

Lake Erie Medical DBA Quality Care Products LLC15 January 2020

Albuterol Sulfate

Albuterol Sulfate Syrup is indicated for the relief of bronchospasm in adults and children 2 years of age and older with reversible obstructive airway disease. CONTRAINDICATIONS: Albuterol Sulfate Syrup is contraindicated in patients with a history…

Lake Erie Medical DBA Quality Care Products LLC4 February 2011

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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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