NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4342Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4342Add 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
70518-4342-07051843420030 TABLET in 1 BOTTLE, PLASTIC (70518-4342-0)Marketed from May 18, 2025
70518-4342-17051843420130 TABLET in 1 BLISTER PACK (70518-4342-1)Marketed from May 19, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 070974
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha2-Agonists (Mechanism)
Identifiers
Product ID 70518-4342_5af86781-9ae4-f05c-e063-6294a90a28b0SPL ID 5af86781-9ae4-f05c-e063-6294a90a28b0SPL set ID 00c6d67a-bb11-4884-9eeb-4e1b8701a08bRxCUI 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

N470518434200 followed by a unit qualifier and the quantity

Package 70518-4342-00. 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 .

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 070974

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

FDA NDC Directory listings under ANDA 070974
ProductStrengthForm · routeLabelerProduct NDC
Clonidine HydrochlorideClonidine hydrochloride .1 mg/1TabletOralREMEDYREPACK INC.70518-1962
Clonidine HydrochlorideClonidine hydrochloride .1 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4661
Clonidine HydrochlorideClonidine hydrochloride .1 mg/1TabletOralActavis Pharma, Inc.0228-2127
Clonidine HydrochlorideClonidine hydrochloride .1 mg/1TabletOralAmerican Health Packaging60687-113
Clonidine HydrochlorideClonidine hydrochloride .1 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-2572
Clonidine HydrochlorideClonidine hydrochloride .1 mg/1TabletOralBluePoint Laboratories68001-237
Clonidine HydrochlorideClonidine hydrochloride .1 mg/1TabletOralNorthwind Health Company, LLC51655-353
Clonidine HydrochlorideClonidine hydrochloride .1 mg/1TabletOralCardinal Health 107, LLC55154-2576
Clonidine HydrochlorideClonidine hydrochloride .1 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2699

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