NDC codes

FDA NDC Directory
Product NDC (as listed)67296-2134Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67296-2134Add 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 NDC11-digit (billing)PackageCopy
67296-2134-66729621340660 mL in 1 BOTTLE, PLASTIC (67296-2134-6)Marketed from Oct 9, 2023

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 Sodium Phosphate
Generic name (nonproprietary)
prednisolone sodium phosphate
Active ingredients
Prednisolone sodium phosphate — 15 mg/5mL
Dosage form
Solution
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203559
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 67296-2134_46aca408-309a-ee64-e063-6294a90a5f4dSPL ID 46aca408-309a-ee64-e063-6294a90a5f4dSPL set ID 3253b63b-0533-6cdc-e063-6294a90aa311RxCUI 283077UNII IV021NXA9JUPC 0342799813011, 0342799816012, 0342799815015, 0342799812014
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N467296213406 followed by a unit qualifier and the quantity

Package 67296-2134-06. 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 .

Indications (excerpt from the label)

INDICATIONS & USAGE Prednisolone Sodium Phosphate Oral Solution (10 mg Prednisolone per 5 mL), Prednisolone Sodium Phosphate Oral Solution (15 mg Prednisolone per 5 mL), Prednisolone Sodium Phosphate Oral Solution (20 mg Prednisolone per 5 mL) and Prednisolone Sodium Phosphate (25 mg Prednisolone per 5 mL) are indicated in the following conditions: 1. Allergic States Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in adult and pediatric populations with: seasonal or perennial allergic rhinitis; asthma; contact dermatitis; atopic dermatitis; serum sickness; drug hypersensitivity reactions. 2. Dermatologic Diseases Pemphigus; bul…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 203559

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

FDA NDC Directory listings under ANDA 203559
ProductStrengthForm · routeLabelerProduct NDC
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralPreferred Pharmaceuticals Inc.68788-4046
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralEdenbridge Pharmaceuticals LLC.42799-815
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 10 mg/5mLSolutionOralEdenbridge Pharmaceuticals LLC.42799-812
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 20 mg/5mLSolutionOralEdenbridge Pharmaceuticals LLC.42799-813
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 25 mg/5mLSolutionOralEdenbridge Pharmaceuticals LLC.42799-816
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralAtlantic Biologicals Corp17856-8815
prednisoLONE sodium phosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralKesin Pharma81033-021
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralATLANTIC BIOLOGICALS CORP.17856-0815

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