Prescription Medications with Generic Names Beginning ‘M’

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Macrilen (Macimorelin Acetate)

MACRILEN is indicated for the diagnosis of adult growth hormone deficiency (AGHD).MACRILEN is a growth hormone (GH) secretagogue receptor agonist indicated for the diagnosis of adult…

Strongbridge U.S. Inc11 January 2019

Macrilen (Macimorelin Acetate)

MACRILEN is indicated for the diagnosis of adult growth hormone deficiency (AGHD).MACRILEN is a growth hormone (GH) secretagogue receptor agonist indicated for the diagnosis of adult…

Novo Nordisk27 November 2019

OPSUMIT (Macitentan)

OPSUMIT is an endothelin receptor antagonist (ERA) indicated for the treatment of pulmonary arterial hypertension (PAH. WHO Group I) to reduce the risks of disease progression and…

Actelion Pharmaceuticals US, Inc.14 January 2021

Mafenide Acetate,USP For 5% Topical Solution is indicated for use as an adjunctive topical antimicrobial agent to control bacterial infection when used under moist dressings over meshed autografts on excised burn wounds. CONTRAINDICATIONS: Mafenide…

Par Pharmaceutical, Inc.10 April 2017

Mafenide Acetate

Mafenide Acetate for 5% Topical Solution is indicated for use as an adjunctive topical antimicrobial agent to control bacterial infection when used under moist dressings over meshed…

Ingenus Pharmaceuticals, LLC21 December 2018

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FDA Medwatch

Nostrum Laboratories, Inc. Expands Voluntary Nationwide Recall of Metformin HCl Extended Release Tablets, USP 750 mg, Due to N-Nitrosodimethylamine (NDMA) Content Above the Acceptable Daily Intake (ADI) Limit
Sun, 24 Jan 2021. Nostrum Laboratories, Inc. is voluntarily recalling one lot of Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) to the consumer level. The Metformin HCl Extended Release Tablets, USP 750 mg (generic…
Boston Scientific Announces LOTUS Edge™ Aortic Valve System Voluntary Recall and Product Discontinuation
Sun, 10 Jan 2021. Boston Scientific Corporation (NYSE: BSX) has announced it has initiated a global, voluntary recall of all unused inventory of the LOTUS Edge™ Aortic Valve System due to complexities associated with the product delivery system. The voluntary…

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As a leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. RxDrugLabels.com provides the full prescription-only subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.