Clonidine Hydrochloride NDC 71335-2489

Product information

Brand name (proprietary)

Clonidine Hydrochloride

Generic name (nonproprietary)

clonidine hydrochloride

Active ingredients

Clonidine hydrochloride — .1 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 71335-2489_a121099c-05a7-4722-b2e2-71eacbfa4cdbSPL ID a121099c-05a7-4722-b2e2-71eacbfa4cdbSPL set ID 1c65bafb-9752-4785-84b1-376cf863fd07RxCUI 884173UNII 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

N471335248900 followed by a unit qualifier and the quantity Copy

Package 71335-2489-00. 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.