clonidine hydrochloride NDC 71335-1495

Product information

Brand name (proprietary)

clonidine hydrochloride

Generic name (nonproprietary)

clonidine hydrochloride

Active ingredients

Clonidine hydrochloride — .2 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 091368

Marketing start

May 3, 2016

Listing expires

Dec 31, 2026

Other FDA classes

Adrenergic alpha2-Agonists (Mechanism)

Identifiers

Product ID 71335-1495_849d5b92-8342-4f52-b280-d0838716a4f0SPL ID 849d5b92-8342-4f52-b280-d0838716a4f0SPL set ID 100a31f2-9a8e-4245-a09c-05583c3244c3RxCUI 884185UNII 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

N471335149501 followed by a unit qualifier and the quantity Copy

Package 71335-1495-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

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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