Finished product reference

Rimegepant

Tablet, Orally Disintegrating · Oral · 75 mg

List code
53652
Salt form
Sulfate

What it is and how it works

Mechanism of Action Rimegepant is a calcitonin gene-related peptide receptor antagonist.

Indications

is a calcitonin gene-related peptide receptor antagonist indicated for the: • acute treatment of migraine with or without aura in adults • preventive treatment of episodic migraine in adults Acute Treatment of Migraine NURTEC ODT is indicated for the acute treatment of migraine with or without aura in adults . Preventive Treatment of Episodic Migraine NURTEC ODT is indicated for the preventive treatment of episodic migraine in adults.

Dosage and administration (summary)

• Recommended dosage for acute treatment of migraine: 75 mg taken orally, as needed. • The safety of using more than 18 doses in a 30-day period has not been established. • Recommended dosage for preventive treatment of episodic migraine: 75 mg taken orally every other day. • The maximum dose in a 24-hour period is 75 mg. • NURTEC ODT can be taken with or without food. ( 2.1 , 2.2 ) Recommended Dosing for Acute Treatment of Migraine The recommended dose of NURTEC ODT is 75 mg taken orally, as needed. The maximum dose in a 24-hour period is 75 mg. The safety of using more than 18 doses in a 30-day period has not been established. NURTEC ODT can be taken with or without food .

Contraindications

is contraindicated in patients with a history of hypersensitivity reaction to rimegepant, NURTEC ODT, or any of its components. Reactions have included anaphylaxis and delayed serious hypersensitivity . Patients with a history of hypersensitivity reaction to rimegepant, NURTEC ODT, or to any of its components.

Warnings and precautions

• Hypersensitivity Reactions: If a serious hypersensitivity reaction occurs, discontinue NURTEC ODT and initiate appropriate therapy. Severe hypersensitivity reactions have included anaphylaxis, dyspnea, and rash, and can occur days after administration. • Hypertension: New-onset or worsening of pre-existing hypertension may occur. • Raynaud’s Phenomenon: New-onset or worsening of pre-existing Raynaud’s phenomenon may occur. Hypersensitivity Reactions Serious hypersensitivity reactions, including anaphylaxis, dyspnea , and rash, have occurred in patients treated with NURTEC ODT .

Pregnancy

Pregnancy Pregnancy Exposure Registry There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to NURTEC ODT during pregnancy. For more information, healthcare providers or patients are encouraged to contact: 1-877-366-0324, email crgnurtecpregnancyregistry@thermofisher.com, or visit nurtecpregnancyregistry.com .

Storage and supply

Storage and Handling Store NURTEC ODT at controlled room temperature, 20°C to 25°C (68°F to 77°F); with excursions permitted between 15°C to 30°C (59°F to 86°F) .

Source: Rimegepant Sulfate (Nurtec Odt) — US FDA prescribing information, 2026-06-04, DailyMed. Summarised and shortened; the full label governs. Iranian registration, indications and labelling may differ.

Reference information for professional sourcing and registration enquiries, not medical advice or a promotion. Drug information is condensed from US FDA prescribing information (public domain, via openFDA and DailyMed) and does not replace the product’s approved labelling in Iran. Availability, origin and documentation are confirmed per enquiry.

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