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
50090-5577_fdd69294-31b5-4a0f-9c9c-210ce908110c
Product NDC
50090-5577
Form
TABLET
Composition / generic term
clonidine hydrochloride
Labeler
A-S Medication Solutions
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

  • 30 TABLET in 1 BOTTLE (50090-5577-0) · 50090-5577-0
  • 60 TABLET in 1 BOTTLE (50090-5577-1) · 50090-5577-1
  • 100 TABLET in 1 BOTTLE (50090-5577-2) · 50090-5577-2
  • 90 TABLET in 1 BOTTLE (50090-5577-7) · 50090-5577-7
  • 180 TABLET in 1 BOTTLE (50090-5577-8) · 50090-5577-8

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 →