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
- 70700-302_23ee7a86-0dc4-c845-93ff-f02aab00ce8f
- Product NDC
- 70700-302
- Form
- TABLET
- Composition / generic term
- Guanfacine Hydrochloride
- Labeler
- XIROMED, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240224
- Source listing expiry
- 20261231
Source-listed ingredients
- GUANFACINE HYDROCHLORIDE — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (70700-302-01) · 70700-302-01
- 500 TABLET in 1 BOTTLE (70700-302-05) · 70700-302-05
- 30 TABLET in 1 BOTTLE (70700-302-30) · 70700-302-30
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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