Prednisolone Acetate NDC 70748-332

NDC codes

FDA NDC Directory

Product NDC (as listed)70748-332Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70748-0332Add 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
70748-332-02	70748033202	1 BOTTLE in 1 CARTON (70748-332-02) / 5 mL in 1 BOTTLEMarketed from Oct 11, 2024
70748-332-03	70748033203	1 BOTTLE in 1 CARTON (70748-332-03) / 10 mL in 1 BOTTLEMarketed from Oct 11, 2024
70748-332-04	70748033204	1 BOTTLE in 1 CARTON (70748-332-04) / 15 mL in 1 BOTTLEMarketed from Oct 11, 2024

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): Prednisolone Acetate
Generic name (nonproprietary): prednisolone acetate
Active ingredients: Prednisolone acetate — 10 mg/mL
Dosage form: Suspension/ drops
Route: Ophthalmic
Labeler: Lupin Pharmaceuticals, Inc.
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 70748-332_8b7144d6-fff1-4afd-a80b-332ff7ed80a1SPL ID 8b7144d6-fff1-4afd-a80b-332ff7ed80a1SPL set ID 75fbeab1-ce8d-4999-a875-472174be5cc6RxCUI 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

N470748033202 followed by a unit qualifier and the quantity

Package 70748-0332-02. 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 Oct 13, 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)

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	Redpharm Drug	67296-2176
Prednisolone Acetate	Prednisolone acetate 10 mg/mL	Suspension/ dropsOphthalmic	A-S Medication Solutions	50090-7539