United States · FDA National Drug Code directory
DOPTELET
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71369-020_4d4d84be-34cd-4027-b69a-2f16ec5049ed
- Product NDC
- 71369-020
- Form
- TABLET, FILM COATED
- Composition / generic term
- avatrombopag maleate
- Labeler
- AkaRx, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20180523
- Source listing expiry
- 20261231
Source-listed ingredients
- AVATROMBOPAG MALEATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (71369-020-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (71369-020-11) · 71369-020-10
- 1 BLISTER PACK in 1 CARTON (71369-020-15) / 15 TABLET, FILM COATED in 1 BLISTER PACK (71369-020-16) · 71369-020-15
- 2 BLISTER PACK in 1 CARTON (71369-020-30) / 15 TABLET, FILM COATED in 1 BLISTER PACK (71369-020-16) · 71369-020-30
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →