Naratriptan how supplied storage and handling

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Naratriptan
NARATRIPTAN tablet® 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

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

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

  1. "NARATRIPTAN TABLET, COATED [SANDOZ INC]".

Adapted from the FDA Package Insert.

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