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Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.

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Naratriptan how supplied storage and handling

Introduction

Naratriptan
NARATRIPTAN tabletÂŽ FDA Package Insert
Indications and Usage
Dosage and Administration
Dosage Forms and Strengths
Contraindications
Warnings and Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Overdosage
Description
Clinical Pharmacology
Nonclinical Toxicology
Clinical Studies
How Supplied/Storage and Handling
Patient Counseling Information
Labels and Packages
Clinical Trials on Naratriptan
ClinicalTrials.gov
How Supplied

How Supplied

Naratriptan tablets, USP are available as follows:

1 mg, white colored ‘D’ shaped, film-coated tablets debossed with ‘SZ’ on one side and ‘247’ on other side

NDC 0781-5526-37 in unit-of-use pack of 9 tablets (1 blister card containing 9 tablets in 1 carton)

2.5 mg, green colored ‘D’ shaped, film-coated tablets debossed with ‘SZ’ on one side and ‘248’ on other side

NDC 0781-5527-37 in unit-of-use pack of 9 tablets (1 blister card containing 9 tablets in 1 carton)

Storage

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].[1]

References

References

  1. ↑ “NARATRIPTAN TABLET, COATED [SANDOZ INC]”.

Adapted from the FDA Package Insert.

Template:Antimigraine preparations

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]