Regorafenib

  • Part D specialty tier in 80% of formularies (2026Q3)
  • Stivarga

Therapy management checklist

Screening, baseline and ongoing monitoring with the label's stated frequency, hold and discontinue criteria, and counseling points, each quoted from the FDA label.

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Storage and cold chain

Regorafenib: storage and handling

Freezing
Not addressed
Room temperature
at or below 30°C (86°F)
Label statement
Store STIVARGA at 25°C (77°F); excursions are permitted from 15 to 30°C (59 to 86°F) [see USP Controlled Room Temperature].
Room temperature
at or below 25°C (77°F)
Label statement
Store STIVARGA tablets at room temperature between 68° F to 77° F (20° C to 25°C).
Back into the refrigerator
Not addressed
Light
Not addressed
Shaking
Not addressed

Temperature excursion helper

Answers only from this label's storage statements. It does not judge whether a product is still usable beyond what the label states.

Within the label's stated room-temperature allowance (at up to 30°C (86°F)). Follow the label's instructions for what to do next.

Entered: 1 day at up to 77°F (25°C).

Store STIVARGA at 25°C (77°F); excursions are permitted from 15 to 30°C (59 to 86°F) [see USP Controlled Room Temperature].
Discard any unused tablets 7 weeks after opening the bottle.
Safely throw away (discard) any unused STIVARGA tablets after 7 weeks of opening the bottle.

If anything else happened to the product, or you are unsure, Contact the manufacturer at 1-888-842-2937 (the number printed on the label) about this product.

Where the label prints this number
For more information, go to www.STIVARGA-US.com or call 1-888-842-2937.
All storage statements on the label (5)
  • Store STIVARGA at 25°C (77°F); excursions are permitted from 15 to 30°C (59 to 86°F) [see USP Controlled Room Temperature].
  • Store tablets in the original bottle and do not remove the desiccant.
  • Discard any unused tablets 7 weeks after opening the bottle.
  • Store STIVARGA tablets at room temperature between 68° F to 77° F (20° C to 25°C).
  • Safely throw away (discard) any unused STIVARGA tablets after 7 weeks of opening the bottle.

FDA label version 36, effective February 9, 2026. DailyMed

Dosing and titration calendar

Built only from the schedules the label states (loading, titration, day schedules, cycles and weight bands). Steps the label states in words the calendar cannot place are shown, not guessed.

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Medicare Part D coverage

100%of plans list it
98%of those: prior authorization
0%step therapy
93%quantity limit
97%specialty tier

5,496 Part D plans, CMS formulary files 2026Q3. Look up tier, PA, step therapy and quantity limits by plan

Patient assistance

No manufacturer program page is listed for this drug yet.

Independent foundations and the full directory (checked 2026-11-06). Eligibility and amounts are set by each program; open its page for them.

For licensed clinicians. Use with clinical judgment. Statements are quoted from the FDA label; confirm against the label for the product you are using.