Chloroprocaine Hydrochloride NDC 84549-209

NDC codes

FDA NDC Directory

Product NDC (as listed)84549-209Labeler and product segments. Claims need a package NDC.

Product NDC at billing width84549-0209Add 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
84549-209-10	84549020910	20 mL in 1 VIAL (84549-209-10)Marketed from Oct 10, 2025

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): Chloroprocaine Hydrochloride
Generic name (nonproprietary): chloroprocaine hydrochloride
Active ingredients: Chloroprocaine hydrochloride — 20 mg/mL
Dosage form: Injection, Solution
Route: Epidural, Infiltration, Intracaudal, Perineural
Labeler: ProPharma Distribution
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 84549-209_463ee055-62a2-9709-e063-6294a90aa7edSPL ID 463ee055-62a2-9709-e063-6294a90aa7edSPL set ID 4305ab6b-6038-9daa-e063-6294a90a018eRxCUI 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

N484549020910 followed by a unit qualifier and the quantity

Package 84549-0209-10. 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 Dec 18, 2025.

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)

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 30 mg/mL	Injection, SolutionEpidural, Infiltration, Intracaudal, Perineural	Hikma Pharmaceuticals USA Inc.	0143-9210