United States · FDA National Drug Code directory
Guanfacine Extended-Release
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
- 71205-946_6de48883-f40b-4aef-83d4-6acb86c1b11e
- Product NDC
- 71205-946
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Guanfacine
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170707
- Source listing expiry
- 20261231
Source-listed ingredients
- GUANFACINE — 3 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-946-00) · 71205-946-00
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-946-30) · 71205-946-30
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-946-55) · 71205-946-55
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-946-60) · 71205-946-60
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-946-90) · 71205-946-90
Source and coverage
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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.
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