United States · FDA National Drug Code directory
Guanfacine Hydrochloride
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
- 29300-458_9df9e7f8-a9b3-4919-94f9-07c81ff7c8b3
- Product NDC
- 29300-458
- Form
- TABLET
- Composition / generic term
- Guanfacine Hydrochloride
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210303
- Source listing expiry
- 20261231
Source-listed ingredients
- GUANFACINE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (29300-458-01) · 29300-458-01
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 →