United States · FDA National Drug Code directory
clonidine 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
- 71335-0777_bc883971-73e7-43b2-8b10-840c87eaa79e
- Product NDC
- 71335-0777
- Form
- TABLET
- Composition / generic term
- Clonidine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160503
- Source listing expiry
- 20261231
Source-listed ingredients
- CLONIDINE HYDROCHLORIDE — .1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 24 TABLET in 1 BOTTLE (71335-0777-0) · 71335-0777-0
- 100 TABLET in 1 BOTTLE (71335-0777-1) · 71335-0777-1
- 30 TABLET in 1 BOTTLE (71335-0777-2) · 71335-0777-2
- 20 TABLET in 1 BOTTLE (71335-0777-3) · 71335-0777-3
- 60 TABLET in 1 BOTTLE (71335-0777-4) · 71335-0777-4
- 120 TABLET in 1 BOTTLE (71335-0777-5) · 71335-0777-5
- 90 TABLET in 1 BOTTLE (71335-0777-6) · 71335-0777-6
- 10 TABLET in 1 BOTTLE (71335-0777-7) · 71335-0777-7
- 45 TABLET in 1 BOTTLE (71335-0777-8) · 71335-0777-8
- 14 TABLET in 1 BOTTLE (71335-0777-9) · 71335-0777-9
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 →