What is NDC 60219-2550?

60219-2550 is the product NDC for prednisolone acetate, Prednisolone acetate 10 mg/mL suspension/ drops, listed with the FDA by Amneal Pharmaceuticals NY LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Amneal Pharmaceuticals NY LLC, NDC labeler code 60219. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for prednisolone acetate?

14 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

prednisolone acetate NDC 60219-2550 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)60219-2550Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60219-2550Add 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
60219-2550-1	60219255001	1 BOTTLE, PLASTIC in 1 CARTON (60219-2550-1) / 5 mL in 1 BOTTLE, PLASTICMarketed from Jun 13, 2025

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): prednisolone acetate
Generic name (nonproprietary): prednisolone acetate
Active ingredients: Prednisolone acetate — 10 mg/mL
Dosage form: Suspension/ drops
Route: Ophthalmic
Labeler: Amneal Pharmaceuticals NY LLCNDC labeler code 60219
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218256
Marketing start: Jun 13, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 60219-2550_b184f928-3c7a-46a0-9c67-7d2946a37868SPL ID b184f928-3c7a-46a0-9c67-7d2946a37868SPL set ID 8d8e8f9b-4d65-426f-8c57-451001cdd849RxCUI 1376336UNII 8B2807733DUPC 0360219255111, 0360219255210
Pharmacologic class: Corticosteroid

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

N460219255001 followed by a unit qualifier and the quantity

Package 60219-2550-01. 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 12, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Prednisolone acetate ophthalmic suspension is indicated for the treatment of steroid-responsive inflammation of the palpebral and bulbar conjunctiva, cornea and anterior segment of the globe.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60219-2550

What is NDC 60219-2550?: 60219-2550 is the product NDC for prednisolone acetate, Prednisolone acetate 10 mg/mL suspension/ drops, listed with the FDA by Amneal Pharmaceuticals NY LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: prednisolone acetate.
What is the active ingredient?: Prednisolone acetate.
Who is the labeler?: Amneal Pharmaceuticals NY LLC, NDC labeler code 60219. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for prednisolone acetate?: 14 other product NDCs are listed under this name. See all prednisolone acetate 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 prednisolone acetate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
prednisolone acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	Amneal Pharmaceuticals NY LLC	60219-2551	60219-2551-01
prednisolone acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	Amneal Pharmaceuticals NY LLC	60219-2552	60219-2552-01
Prednisolone Acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	A-S Medication Solutions	50090-7539	50090-7539-00
Prednisolone Acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	Lupin Pharmaceuticals, Inc.	70748-332	70748-0332-0270748-0332-0370748-0332-04
Prednisolone Acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	Redpharm Drug	67296-2176	67296-2176-05
Prednisolone Acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	Pacific Pharma, Inc.	60758-119	60758-0119-0560758-0119-1060758-0119-15
Prednisolone Acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	Asclemed USA, Inc.	76420-204	76420-0204-05
Prednisolone Acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	A-S Medication Solutions	50090-5275	50090-5275-00
Prednisolone Acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	NuCare Pharmaceuticals,Inc.	68071-2222	68071-2222-05
Prednisolone Acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	A-S Medication Solutions	50090-1912	50090-1912-00

All 15 prednisolone acetate NDCs

Other NDCs under ANDA 218256

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

FDA NDC Directory listings under ANDA 218256
Product	Strength	Form · route	Labeler	Product NDC
prednisolone acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	Amneal Pharmaceuticals NY LLC	60219-2551
prednisolone acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	Amneal Pharmaceuticals NY LLC	60219-2552