What is NDC 0143-9210?

0143-9210 is the product NDC for Chloroprocaine Hydrochloride, Chloroprocaine hydrochloride 30 mg/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 Chloroprocaine Hydrochloride?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Chloroprocaine Hydrochloride NDC 0143-9210

NDC codes

FDA NDC Directory

Product NDC (as listed)0143-9210Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00143-9210Add 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
0143-9210-10	0014392101000143921010	10 VIAL in 1 CARTON (0143-9210-10) / 20 mL in 1 VIAL (0143-9210-01)Marketed from Nov 1, 1998

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): Chloroprocaine Hydrochloride
Generic name (nonproprietary): chloroprocaine hydrochloride
Active ingredients: Chloroprocaine hydrochloride — 30 mg/mL
Dosage form: Injection, Solution
Route: Epidural, Infiltration, Intracaudal, Perineural
Labeler: Hikma Pharmaceuticals USA Inc.NDC labeler code 0143
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040273
Marketing start: Nov 1, 1998
Listing expires: Dec 31, 2026
Other FDA classes: Esters (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers: Product ID 0143-9210_a652f290-f8c6-4483-9fe4-b1fd50dec37dSPL ID a652f290-f8c6-4483-9fe4-b1fd50dec37dSPL set ID e21e24d5-0535-4962-b9ed-7957fe4ed3dbRxCUI 992809, 1794184UNII LT7Z1YW11H
Pharmacologic class: Ester Local Anesthetic

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.

NDC on a medical claim

N400143921010 followed by a unit qualifier and the quantity

Package 00143-9210-10. 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 Feb 25, 2022.

Indications (excerpt from the label)

INDICATIONS AND USAGE Chloroprocaine hydrochloride injection 2% and 3%, in single dose vials, without methylparaben preservative, without EDTA, is indicated for the production of local anesthesia by infiltration, peripheral and central nerve block, including lumbar and caudal epidural blocks. Chloroprocaine hydrochloride injection is not to be used for subarachnoid administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0143-9210

What is NDC 0143-9210?: 0143-9210 is the product NDC for Chloroprocaine Hydrochloride, Chloroprocaine hydrochloride 30 mg/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?: Chloroprocaine Hydrochloride.
What is the active ingredient?: Chloroprocaine 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 Chloroprocaine Hydrochloride?: 2 other product NDCs are listed under this name. See all Chloroprocaine 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 Chloroprocaine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Chloroprocaine Hydrochloride	Chloroprocaine hydrochloride 20 mg/mL	Injection, SolutionEpidural, Infiltration, Intracaudal, Perineural	Hikma Pharmaceuticals USA Inc.	0143-9209	00143-9209-10
Chloroprocaine Hydrochloride	Chloroprocaine hydrochloride 20 mg/mL	Injection, SolutionEpidural, Infiltration, Intracaudal, Perineural	ProPharma Distribution	84549-209	84549-0209-10

Other NDCs under ANDA 040273

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

FDA NDC Directory listings under ANDA 040273
Product	Strength	Form · route	Labeler	Product NDC
Chloroprocaine Hydrochloride	Chloroprocaine hydrochloride 20 mg/mL	Injection, SolutionEpidural, Infiltration, Intracaudal, Perineural	Hikma Pharmaceuticals USA Inc.	0143-9209
Chloroprocaine Hydrochloride	Chloroprocaine hydrochloride 20 mg/mL	Injection, SolutionEpidural, Infiltration, Intracaudal, Perineural	ProPharma Distribution	84549-209