NDC codes

FDA NDC Directory
Product NDC (as listed)71610-449Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71610-0449Add 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
71610-449-0971610044909716100449099000 TABLET in 1 BOTTLE (71610-449-09)Marketed from Jul 28, 2020

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
Aphena Pharma Solutions - Tennessee, LLCNDC labeler code 71610
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 71610-449_6e5cec35-31fa-4db7-a681-cd264ebd6cbfSPL ID 6e5cec35-31fa-4db7-a681-cd264ebd6cbfSPL set ID 00d1562d-b4eb-4d89-95de-0aacee7a82a5RxCUI 884189UNII 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

N471610044909 followed by a unit qualifier and the quantity

Package 71610-0449-09. 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)

About NDC 71610-449

What is NDC 71610-449?
71610-449 is the product NDC for Clonidine hydrochloride, Clonidine hydrochloride .3 mg/1 tablet, listed with the FDA by Aphena Pharma Solutions - Tennessee, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Clonidine hydrochloride.
What is the active ingredient?
Clonidine hydrochloride.
Who is the labeler?
Aphena Pharma Solutions - Tennessee, LLC, NDC labeler code 71610. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Clonidine hydrochloride?
140 other product NDCs are listed under this name. See all Clonidine hydrochloride NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Clonidine hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
clonidine hydrochlorideClonidine hydrochloride .05 mg/1TabletOralAlembic Pharmaceuticals Inc.62332-16962332-0169-1062332-0169-3062332-0169-31+3 more
clonidine hydrochlorideClonidine hydrochloride .3 mg/1TabletOralCoupler LLC67046-064667046-0646-03
Clonidine HydrochlorideClonidine hydrochloride .2 mg/1TabletOralUnit Dose Solutions, Inc.87441-02487441-0024-01
Clonidine hydrochlorideClonidine hydrochloride .1 mg/1TabletOralUnit Dose Solutions, Inc.87441-02387441-0023-01
Clonidine hydrochlorideClonidine hydrochloride .05 mg/1TabletOralTruPharma, LLC52817-18352817-0183-10
Clonidine HydrochlorideClonidine hydrochloride .2 mg/1TabletOralMajor Pharmaceuticals0904-744300904-7443-61
Clonidine HydrochlorideClonidine hydrochloride .1 mg/1TabletOralCardinal Health 107, LLC55154-018955154-0189-00
Clonidine HydrochlorideClonidine hydrochloride .3 mg/1TabletOralREMEDYREPACK INC.70518-437970518-4379-00
Clonidine HydrochlorideClonidine hydrochloride .2 mg/1TabletOralREMEDYREPACK INC.70518-435770518-4357-00
Clonidine HydrochlorideClonidine hydrochloride .1 mg/1TabletOralREMEDYREPACK INC.70518-434270518-4342-0070518-4342-01

All 141 Clonidine hydrochloride NDCs

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/1TabletOralNorthwind Health Company, LLC51655-451
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/1TabletOralAsclemed USA, Inc.76420-286
Clonidine hydrochlorideClonidine hydrochloride .1 mg/1TabletOralUnit Dose Solutions, Inc.87441-023

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