Clonidine Hydrochloride NDC 71335-9682

Product information

Brand name (proprietary)

Clonidine Hydrochloride

Generic name (nonproprietary)

clonidine hydrochloride

Active ingredients

Clonidine hydrochloride — .3 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 202297

Marketing start

Jul 1, 2020

Listing expires

Dec 31, 2026

Other FDA classes

Adrenergic alpha2-Agonists (Mechanism)

Identifiers

Product ID 71335-9682_652ef659-0000-41d2-8fdb-b4dcd4105c17SPL ID 652ef659-0000-41d2-8fdb-b4dcd4105c17SPL set ID 075b6261-9064-41da-b5e0-0959767e0d9aRxCUI 884189UNII W76I6XXF06

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

N471335968201 followed by a unit qualifier and the quantity Copy

Package 71335-9682-01. 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

Other NDCs under ANDA 202297

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