NDC codes

FDA NDC Directory
Product NDC (as listed)71205-588Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0588Add 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
71205-588-12712050588127120505881212 TABLET in 1 BOTTLE (71205-588-12)Marketed from Jul 7, 2021
71205-588-30712050588307120505883030 TABLET in 1 BOTTLE (71205-588-30)Marketed from Jul 7, 2021
71205-588-60712050588607120505886060 TABLET in 1 BOTTLE (71205-588-60)Marketed from Jul 7, 2021
71205-588-90712050588907120505889090 TABLET in 1 BOTTLE (71205-588-90)Marketed from Jul 7, 2021

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
Labeler
Proficient Rx LPNDC labeler code 71205
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 070925
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha2-Agonists (Mechanism)
Identifiers
Product ID 71205-588_63ed2151-a687-4972-bbe7-f1f1ec060659SPL ID 63ed2151-a687-4972-bbe7-f1f1ec060659SPL set ID 33c68d5e-6a68-40fd-a326-bf36a7e01d5bRxCUI 884173UNII W76I6XXF06UPC 0371205588304
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

N471205058812 followed by a unit qualifier and the quantity

Package 71205-0588-12. 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 71205-588

What is NDC 71205-588?
71205-588 is the product NDC for Clonidine hydrochloride, Clonidine hydrochloride .1 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 4 package NDCs, 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?
Proficient Rx LP, NDC labeler code 71205. 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 070925

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

FDA NDC Directory listings under ANDA 070925
ProductStrengthForm · routeLabelerProduct NDC
Clonidine hydrochlorideClonidine hydrochloride .1 mg/1TabletOralNorthwind Health Company, LLC51655-445
Clonidine HydrochlorideClonidine hydrochloride .1 mg/1TabletOralProficient Rx LP63187-202
Clonidine hydrochlorideClonidine hydrochloride .1 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3987
Clonidine hydrochlorideClonidine hydrochloride .1 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4545
Clonidine hydrochlorideClonidine hydrochloride .1 mg/1TabletOralBryant Ranch Prepack71335-0922
Clonidine hydrochlorideClonidine hydrochloride .1 mg/1TabletOralAsclemed USA, Inc.76420-283

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