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
- 71335-2266_b9bc9103-8bb5-4ff2-a188-a2ed60d7ef2e
- Product NDC
- 71335-2266
- Form
- TABLET
- Composition / generic term
- clonidine hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201224
- 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, PLASTIC (71335-2266-0) · 71335-2266-0
- 100 TABLET in 1 BOTTLE, PLASTIC (71335-2266-1) · 71335-2266-1
- 30 TABLET in 1 BOTTLE, PLASTIC (71335-2266-2) · 71335-2266-2
- 20 TABLET in 1 BOTTLE, PLASTIC (71335-2266-3) · 71335-2266-3
- 60 TABLET in 1 BOTTLE, PLASTIC (71335-2266-4) · 71335-2266-4
- 120 TABLET in 1 BOTTLE, PLASTIC (71335-2266-5) · 71335-2266-5
- 90 TABLET in 1 BOTTLE, PLASTIC (71335-2266-6) · 71335-2266-6
- 10 TABLET in 1 BOTTLE, PLASTIC (71335-2266-7) · 71335-2266-7
- 45 TABLET in 1 BOTTLE, PLASTIC (71335-2266-8) · 71335-2266-8
- 14 TABLET in 1 BOTTLE, PLASTIC (71335-2266-9) · 71335-2266-9
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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