NDC codes

FDA NDC Directory
Product NDC (as listed)87441-023Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87441-0023Add 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
87441-023-018744100230130 TABLET in 1 BLISTER PACK (87441-023-01)Marketed from Jun 15, 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 — .1 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 070923
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha2-Agonists (Mechanism)
Identifiers
Product ID 87441-023_544eb617-ea1f-edf8-e063-6394a90afc72SPL ID 544eb617-ea1f-edf8-e063-6394a90afc72SPL set ID 544ea5bf-6713-f034-e063-6394a90a781bRxCUI 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

N487441002301 followed by a unit qualifier and the quantity

Package 87441-0023-01. 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 USP are indicated in the treatment of hypertension. Clonidine hydrochloride tablets USP 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 070923

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

FDA NDC Directory listings under ANDA 070923
ProductStrengthForm · routeLabelerProduct NDC
Clonidine hydrochlorideClonidine hydrochloride .3 mg/1TabletOralAsclemed USA, Inc.76420-286
Clonidine hydrochlorideClonidine hydrochloride .1 mg/1TabletOralTruPharma, LLC52817-180
Clonidine hydrochlorideClonidine hydrochloride .2 mg/1TabletOralTruPharma, LLC52817-181
Clonidine hydrochlorideClonidine hydrochloride .3 mg/1TabletOralTruPharma, LLC52817-182
Clonidine hydrochlorideClonidine hydrochloride .05 mg/1TabletOralTruPharma, LLC52817-183
Clonidine hydrochlorideClonidine hydrochloride .3 mg/1TabletOralBryant Ranch Prepack71335-1624
Clonidine hydrochlorideClonidine hydrochloride .3 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-449
Clonidine hydrochlorideClonidine hydrochloride .3 mg/1TabletOralNorthwind Health Company, LLC51655-451

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