NDC codes

FDA NDC Directory
Product NDC (as listed)87441-024Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87441-0024Add 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 NDC11-digit (billing)PackageCopy
87441-024-018744100240130 TABLET in 1 BLISTER PACK (87441-024-01)Marketed from Jun 17, 2026

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 — .2 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 070975
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha2-Agonists (Mechanism)
Identifiers
Product ID 87441-024_547bdccc-80e9-3da1-e063-6394a90ab6d8SPL ID 547bdccc-80e9-3da1-e063-6394a90ab6d8SPL set ID 547beb0f-0c12-2ef4-e063-6394a90a6a73RxCUI 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

N487441002401 followed by a unit qualifier and the quantity

Package 87441-0024-01. 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

Current FDA label (SPL), effective .

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 070975

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

FDA NDC Directory listings under ANDA 070975
ProductStrengthForm · routeLabelerProduct NDC
Clonidine HydrochlorideClonidine hydrochloride .2 mg/1TabletOralAmerican Health Packaging60687-124
Clonidine HydrochlorideClonidine hydrochloride .2 mg/1TabletOralActavis Pharma, Inc.0228-2128
Clonidine HydrochlorideClonidine hydrochloride .2 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8272
Clonidine HydrochlorideClonidine hydrochloride .2 mg/1TabletOralBluePoint Laboratories68001-238
Clonidine HydrochlorideClonidine hydrochloride .2 mg/1TabletOralREMEDYREPACK INC.70518-4357
Clonidine HydrochlorideClonidine hydrochloride .2 mg/1TabletOralCoupler LLC67046-1000
Clonidine HydrochlorideClonidine hydrochloride .2 mg/1TabletOralNorthwind Health Company, LLC51655-362
Clonidine HydrochlorideClonidine hydrochloride .2 mg/1TabletOralCardinal Health 107, LLC55154-2577

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