United States · FDA National Drug Code directory

guanfacine

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
0228-2850_00143252-2b74-4b11-86ed-9b864635f129
Product NDC
0228-2850
Form
TABLET, EXTENDED RELEASE
Composition / generic term
guanfacine
Labeler
Actavis Pharma, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20141201 / 20270531

Source-listed ingredients

  • GUANFACINE HYDROCHLORIDE — 1 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0228-2850-11) · 0228-2850-11

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.

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guanfacine — United States | Molindra Medicines