clonidine hydrochloride NDC 62332-169

Product information

Brand name (proprietary)

clonidine hydrochloride

Generic name (nonproprietary)

clonidine hydrochloride

Active ingredients

Clonidine hydrochloride — .05 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Alembic Pharmaceuticals Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 091368

Marketing start

Sep 22, 2026

Listing expires

Dec 31, 2027

Other FDA classes

Adrenergic alpha2-Agonists (Mechanism)

Identifiers

Product ID 62332-169_f3d64f9f-6bfb-48e8-aed1-5623415005edSPL ID f3d64f9f-6bfb-48e8-aed1-5623415005ed

Pharmacologic class

Central alpha-2 Adrenergic Agonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N462332016910 followed by a unit qualifier and the quantity Copy

Package 62332-0169-10. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 091368

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

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