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
- 70518-1962_5332cdd6-bd19-da82-e063-6294a90a7d1b
- Product NDC
- 70518-1962
- Form
- TABLET
- Composition / generic term
- Clonidine Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190318
- Source listing expiry
- 20271231
Source-listed ingredients
- CLONIDINE HYDROCHLORIDE — .1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 POUCH in 1 BOX (70518-1962-6) / 1 TABLET in 1 POUCH (70518-1962-7) · 70518-1962-6
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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