NDC codes

FDA NDC Directory
Product NDC (as listed)17856-8815Labeler and product segments. Claims need a package NDC.
Product NDC at billing width17856-8815Add 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
17856-8815-1178568815011785688150150 CUP, UNIT-DOSE in 1 CASE (17856-8815-1) / 5 mL in 1 CUP, UNIT-DOSEMarketed from Oct 1, 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 Sodium Phosphate
Generic name (nonproprietary)
prednisolone sodium phosphate
Active ingredients
Prednisolone sodium phosphate — 15 mg/5mL
Dosage form
Solution
Route
Oral
Labeler
Atlantic Biologicals CorpNDC labeler code 17856
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 17856-8815_401f96d7-592c-5df2-e063-6294a90a104dSPL ID 401f96d7-592c-5df2-e063-6294a90a104dSPL set ID 401f7ba6-a4a2-9ae6-e063-6394a90a4210RxCUI 283077UNII IV021NXA9J
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

N417856881501 followed by a unit qualifier and the quantity

Package 17856-8815-01. 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 .

Indications (excerpt from the label)

INDICATIONS & USAGE Prednisolone Sodium Phosphate Oral Solution (15 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; bullous dermatitis herpetiformis; severe erythema multiforme (Stevens-Johnson syndrome); exfoliative erythroderma; mycosis fungoides. 3. Edematous States To induce diuresis or remission of proteinuria in nephrotic syn…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17856-8815

What is NDC 17856-8815?
17856-8815 is the product NDC for Prednisolone Sodium Phosphate, Prednisolone sodium phosphate 15 mg/5mL solution, listed with the FDA by Atlantic Biologicals Corp. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Prednisolone Sodium Phosphate.
What is the active ingredient?
Prednisolone sodium phosphate.
Who is the labeler?
Atlantic Biologicals Corp, NDC labeler code 17856. 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 Sodium Phosphate?
21 other product NDCs are listed under this name. See all Prednisolone Sodium Phosphate 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 Sodium Phosphate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
PrednisoLONE Sodium PhosphatePrednisolone sodium phosphate 5 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-110000121-1100-04
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralREMEDYREPACK INC.70518-452470518-4524-0070518-4524-0270518-4524-04
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralPreferred Pharmaceuticals Inc.68788-404668788-4046-02
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralPAI Holdings, LLC dba PAI Pharma0121-475900121-4759-50
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralATLANTIC BIOLOGICALS CORP.17856-081517856-0815-0117856-0815-0217856-0815-03+1 more
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralEdenbridge Pharmaceuticals LLC.42799-81542799-0815-01
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralRedpharm Drug67296-213467296-2134-06
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 25 mg/5mLSolutionOralEdenbridge Pharmaceuticals LLC.42799-81642799-0816-01
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralAmneal Pharmaceuticals NY LLC69238-212269238-2122-09
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralPreferred Pharmaceuticals, Inc.68788-770868788-7708-02

All 22 Prednisolone Sodium Phosphate NDCs

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/5mLSolutionOralATLANTIC BIOLOGICALS CORP.17856-0815
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 15 mg/5mLSolutionOralEdenbridge Pharmaceuticals LLC.42799-815
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 25 mg/5mLSolutionOralEdenbridge Pharmaceuticals LLC.42799-816
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralRedpharm Drug67296-2134
Prednisolone Sodium PhosphatePrednisolone sodium phosphate 15 mg/5mLSolutionOralPreferred Pharmaceuticals Inc.68788-4046

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