Clonidine Hydrochloride NDC 68001-239

NDC codes

FDA NDC Directory

Product NDC (as listed)68001-239Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68001-0239Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
68001-239-00	68001023900	100 TABLET in 1 BOTTLE (68001-239-00)Marketed from Jan 3, 1995

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

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: BluePoint Laboratories
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 070976
Marketing start: Jan 3, 1995
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha2-Agonists (Mechanism)
Identifiers: Product ID 68001-239_42c4b1f4-a2c5-e21f-e063-6294a90aa481SPL ID 42c4b1f4-a2c5-e21f-e063-6294a90aa481SPL set ID 1ea412db-d847-4094-be83-e3bd7328537aRxCUI 884173, 884185, 884189UNII W76I6XXF06UPC 0368001239004, 0368001238007, 0368001237000
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

N468001023900 followed by a unit qualifier and the quantity

Package 68001-0239-00. 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

Current FDA label (SPL), effective Nov 4, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Clonidine hydrochloride tablets are indicated in the treatment of hypertension. Clonidine hydrochloride tablets may be employed alone or concomitantly with other antihypertensive agents.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 070976

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

FDA NDC Directory listings under ANDA 070976
Product	Strength	Form · route	Labeler	Product NDC
Clonidine Hydrochloride	Clonidine hydrochloride .3 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	43353-316
Clonidine Hydrochloride	Clonidine hydrochloride .3 mg/1	TabletOral	Actavis Pharma, Inc.	0228-2129
Clonidine Hydrochloride	Clonidine hydrochloride .3 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-2574