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Pfizer Recalls Nurtec ODT Prescription Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

  • Recalled Nurtec® ODT (rimegepant) orally disintegrating tablets

  • Recalled Nurtec® ODT (rimegepant) orally disintegrating tablets (blister packaging)

Name of Product:

Nurtec® ODT (rimegepant) orally disintegrating tablets, 75mg 8-Unit Dose blister pack


The recalled prescription drugs must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.

Recall Date:

March 16, 2023

Recall Details


This recall involves prescription drugs Nurtec ODT 75 mg orally disintegrating tablets sold in cartons containing one blister card of 8 tablets. The tablets are in a non-child resistant blister card packaged in a carton that includes the name of the product, dosage strength, NDC number and expiration date. The dosage strength and expiration date are printed or stamped on the blister card.

The recall includes the following:

Product Description

NDC Number

Expiration Date

Nurtec® ODT (rimegepant) 75mg 8-Unit Dose blister pack


All dates through 6/2026



Consumers should immediately secure the recalled product out of the sight and reach of children and contact Pfizer for a free child resistant pouch to store the product. Once the product is secured, consumers can continue to use it as directed.

Sold At:

Pharmacies nationwide as a prescribed medicine from December 2021 through March 2023. The prices of the product varied based on health insurance terms and other factors.


Biohaven Pharmaceuticals Inc., of New Haven, Conn. and Pfizer Inc., of New York

Manufactured In:

United States

Report an unsafe product

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