What is NDC 0143-9724?

0143-9724 is the product NDC for Clonidine Hydrochloride, Clonidine hydrochloride 100 ug/mL injection, solution, listed with the FDA by Hikma Pharmaceuticals USA Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Hikma Pharmaceuticals USA Inc., NDC labeler code 0143. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Clonidine Hydrochloride NDC 0143-9724

NDC codes

FDA NDC Directory

Product NDC (as listed)0143-9724Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00143-9724Add 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 NDC	11-digit (billing)	Package	Copy
0143-9724-01	0014397240100143972401	10 mL in 1 VIAL, SINGLE-USE (0143-9724-01)Marketed from Jan 1, 2011

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 100 ug/mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: Hikma Pharmaceuticals USA Inc.NDC labeler code 0143
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 200300
Marketing start: Jan 1, 2011
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha2-Agonists (Mechanism)
Identifiers: Product ID 0143-9724_9d6244d1-5e85-4da3-b06c-f4fe8da1b6faSPL ID 9d6244d1-5e85-4da3-b06c-f4fe8da1b6faSPL set ID 2a5b46ec-4c16-48a5-9e58-8d28a3f21274RxCUI 884221, 884225UNII 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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N400143972401 followed by a unit qualifier and the quantity

Package 00143-9724-01. 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 Jun 27, 2022.

Indications (excerpt from the label)

INDICATIONS AND USAGE Clonidine Hydrochloride Injection, USP is indicated in combination with opiates for the treatment of severe pain in cancer patients that is not adequately relieved by opioid analgesics alone. Epidural clonidine is more likely to be effective in patients with neuropathic pain than somatic or visceral pain (see CLINICAL PHARMACOLOGY: Clinical Trials ). The safety of this drug product has only been established in a highly selected group of cancer patients, and only after an adequate trial of opioid analgesia. Other use is of unproven safety and is not recommended. In a rare patient, the potential benefits may outweigh the known risks (see WARNINGS ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0143-9724

What is NDC 0143-9724?: 0143-9724 is the product NDC for Clonidine Hydrochloride, Clonidine hydrochloride 100 ug/mL injection, solution, listed with the FDA by Hikma Pharmaceuticals USA Inc.. 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?: Hikma Pharmaceuticals USA Inc., NDC labeler code 0143. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
clonidine hydrochloride	Clonidine hydrochloride .05 mg/1	TabletOral	Alembic Pharmaceuticals Inc.	62332-169	62332-0169-1062332-0169-3062332-0169-31+3 more
clonidine hydrochloride	Clonidine hydrochloride .3 mg/1	TabletOral	Coupler LLC	67046-0646	67046-0646-03
Clonidine Hydrochloride	Clonidine hydrochloride .2 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-024	87441-0024-01
Clonidine hydrochloride	Clonidine hydrochloride .1 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-023	87441-0023-01
Clonidine hydrochloride	Clonidine hydrochloride .05 mg/1	TabletOral	TruPharma, LLC	52817-183	52817-0183-10
Clonidine Hydrochloride	Clonidine hydrochloride .2 mg/1	TabletOral	Major Pharmaceuticals	0904-7443	00904-7443-61
Clonidine Hydrochloride	Clonidine hydrochloride .1 mg/1	TabletOral	Cardinal Health 107, LLC	55154-0189	55154-0189-00
Clonidine Hydrochloride	Clonidine hydrochloride .3 mg/1	TabletOral	REMEDYREPACK INC.	70518-4379	70518-4379-00
Clonidine Hydrochloride	Clonidine hydrochloride .2 mg/1	TabletOral	REMEDYREPACK INC.	70518-4357	70518-4357-00
Clonidine Hydrochloride	Clonidine hydrochloride .1 mg/1	TabletOral	REMEDYREPACK INC.	70518-4342	70518-4342-0070518-4342-01

All 141 Clonidine Hydrochloride NDCs

Other NDCs under ANDA 200300

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

FDA NDC Directory listings under ANDA 200300
Product	Strength	Form · route	Labeler	Product NDC
Clonidine Hci	Clonidine hydrochloride 100 ug/mL	Injection, SolutionIntravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1346
Clonidine Hydrochloride	Clonidine hydrochloride 500 ug/mL	Injection, SolutionIntravenous	Hikma Pharmaceuticals USA Inc.	0143-9723