What is NDC 48102-053?

48102-053 is the product NDC for Phospholine Iodide kit, listed with the FDA by Fera Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Phospholine Iodide (Echothiophate iodide for ophthalmic solution).

Fera Pharmaceuticals, LLC, NDC labeler code 48102. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Phospholine Iodide?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Phospholine Iodide NDC 48102-053 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)48102-053Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48102-0053Add 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
48102-053-05	48102005305	1 KIT in 1 CARTON (48102-053-05) * 6.25 mL in 1 BOTTLE (48102-054-05) * 5 mL in 1 BOTTLE (48102-055-05)Marketed from Jun 1, 2022

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): Phospholine Iodide
Generic name (nonproprietary): echothiophate iodide for ophthalmic solution
Dosage form: Kit
Route: Ophthalmic
Labeler: Fera Pharmaceuticals, LLCNDC labeler code 48102
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 011963
Marketing start: Jun 1, 2022
Listing expires: Dec 31, 2026
Identifiers: Product ID 48102-053_66abcfcf-b16e-4181-b1db-96bfba0ab95eSPL ID 66abcfcf-b16e-4181-b1db-96bfba0ab95eSPL set ID 8afc8951-db76-4f27-8752-7c0d6aa47244RxCUI 205739, 310049UPC 0348102053051

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

N448102005305 followed by a unit qualifier and the quantity

Package 48102-0053-05. 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 Jul 7, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Reduction of Elevated IOP Echothiophate iodide for ophthalmic solution is indicated for the reduction of elevated IOP. Accommodative Esotropia Concomitant esotropias with a significant accommodative component.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 48102-053

What is NDC 48102-053?: 48102-053 is the product NDC for Phospholine Iodide kit, listed with the FDA by Fera Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Phospholine Iodide (Echothiophate iodide for ophthalmic solution).
Who is the labeler?: Fera Pharmaceuticals, LLC, NDC labeler code 48102. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Phospholine Iodide?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.