United States · FDA National Drug Code directory
Clonidine
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
- 50742-247_4f2ad773-518b-4532-bb69-8ff28c4f24c4
- Product NDC
- 50742-247
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- clonidine
- Labeler
- Ingenus Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190305
- Source listing expiry
- 20261231
Source-listed ingredients
- CLONIDINE HYDROCHLORIDE — .1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-05) · 50742-247-05
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-30) · 50742-247-30
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-60) · 50742-247-60
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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