Proparacaine Hydrochloride NDC 70518-3408

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-3408Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-3408Add 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
70518-3408-0	70518340800	1 BOTTLE in 1 CARTON (70518-3408-0) / 15 mL in 1 BOTTLEMarketed from Apr 8, 2022

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): Proparacaine Hydrochloride
Generic name (nonproprietary): proparacaine hydrochloride
Active ingredients: Proparacaine hydrochloride — 5 mg/mL
Dosage form: Solution/ drops
Route: Ophthalmic
Labeler: REMEDYREPACK INC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 080027
Marketing start: Apr 8, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Local Anesthesia (Physiologic effect)
Identifiers: Product ID 70518-3408_4f067d6e-665e-c24f-e063-6294a90ab03eSPL ID 4f067d6e-665e-c24f-e063-6294a90ab03eSPL set ID 55ed1359-d95c-4c2b-ad5a-cc8e023c4331RxCUI 1191013UNII U96OL57GOY
Pharmacologic class: 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 HCPCS code in Med-Code's directory. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470518340800 followed by a unit qualifier and the quantity

Package 70518-3408-00. 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 Apr 9, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Proparacaine hydrochloride ophthalmic solution is indicated for procedures in which a topical ophthalmic anesthetic is indicated: corneal anesthesia of short duration, e.g. tonometry, gonioscopy, removal of corneal foreign bodies, and for short corneal and conjunctival procedures.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 080027

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

FDA NDC Directory listings under ANDA 080027
Product	Strength	Form · route	Labeler	Product NDC
Alcaineproparacaine hydrochloride	Proparacaine hydrochloride 5 mg/mL	Solution/ dropsOphthalmic	Alcon Laboratories, Inc.	0998-0016
proparacaine hydrochloride	Proparacaine hydrochloride 5 mg/mL	Solution/ dropsOphthalmic	NuCare Pharmaceuticals,Inc.	68071-5139
Proparacaine Hydrochloride	Proparacaine hydrochloride 5 mg/mL	Solution/ dropsOphthalmic	Sportpharm LLC	85766-056
Proparacaine Hydrochloride	Proparacaine hydrochloride 5 mg/mL	Solution/ dropsOphthalmic	Sandoz Inc.	61314-016