What is NDC 67296-2176?

67296-2176 is the product NDC for Prednisolone Acetate, Prednisolone acetate 10 mg/mL suspension/ drops, listed with the FDA by Redpharm Drug. It has 1 package NDC, shown above in 10- and 11-digit form.

Redpharm Drug, NDC labeler code 67296. 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 67296-2176 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)67296-2176Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67296-2176Add 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
67296-2176-5	67296217605	1 BOTTLE in 1 CARTON (67296-2176-5) / 5 mL in 1 BOTTLEMarketed from Oct 11, 2024

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: Redpharm DrugNDC labeler code 67296
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 216935
Marketing start: Oct 11, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 67296-2176_44f6dd75-df38-6985-e063-6294a90a80cdSPL ID 44f6dd75-df38-6985-e063-6294a90a80cdSPL set ID 3dd0195c-8522-bbf9-e063-6394a90a9f3eRxCUI 1376336UNII 8B2807733D
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

N467296217605 followed by a unit qualifier and the quantity

Package 67296-2176-05. 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 Dec 2, 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 67296-2176

What is NDC 67296-2176?: 67296-2176 is the product NDC for Prednisolone Acetate, Prednisolone acetate 10 mg/mL suspension/ drops, listed with the FDA by Redpharm Drug. 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?: Redpharm Drug, NDC labeler code 67296. 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	60219-2550	60219-2550-01
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	A-S Medication Solutions	50090-1912	50090-1912-00
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	Pacific Pharma, Inc.	60758-119	60758-0119-0560758-0119-1060758-0119-15
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	Asclemed USA, Inc.	76420-204	76420-0204-05

All 15 Prednisolone Acetate NDCs

Other NDCs under ANDA 216935

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

FDA NDC Directory listings under ANDA 216935
Product	Strength	Form · route	Labeler	Product NDC
Prednisolone Acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	A-S Medication Solutions	50090-7539
Prednisolone Acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	Lupin Pharmaceuticals, Inc.	70748-332