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
- 27241-108_ab37a98e-cfb2-4aca-92da-68dedfb13657
- Product NDC
- 27241-108
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Clonidine hydrochloride
- Labeler
- Ajanta Pharma USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171121
- Source listing expiry
- 20261231
Source-listed ingredients
- CLONIDINE HYDROCHLORIDE — .1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-108-06) · 27241-108-06
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 →