Prescription drug · ANDA
Prednisolone Sodium Phosphate NDC 68999-330
Prednisolone sodium phosphate 5 mg/5mL · Solution · Oral · Chartwell Governmental & Specialty RX, LLC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68999-330-24 | 6899903302468999033024 | 2 TRAY in 1 BOX (68999-330-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-330-05)Marketed from Nov 26, 2025 |
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 Sodium Phosphate
- Generic name (nonproprietary)
- prednisolone sodium phosphate
- Active ingredients
- Prednisolone sodium phosphate — 5 mg/5mL
- Dosage form
- Solution
- Route
- Oral
- Labeler
- Chartwell Governmental & Specialty RX, LLC.NDC labeler code 68999
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 075988
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 68999-330_453ad2a6-3423-b21b-e063-6294a90abb44SPL ID 453ad2a6-3423-b21b-e063-6294a90abb44SPL set ID 5ec401b5-132a-4cd2-8c24-6a5c8b63c2f9RxCUI 312614UNII 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
N468999033024followed by a unit qualifier and the quantityPackage 68999-0330-24. 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 AND USAGE Prednisolone sodium phosphate oral solution is 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 syndrome in adults with lupus er…
Excerpt only. Read the full label for complete information.
About NDC 68999-330
- What is NDC 68999-330?
- 68999-330 is the product NDC for Prednisolone Sodium Phosphate, Prednisolone sodium phosphate 5 mg/5mL solution, listed with the FDA by Chartwell Governmental & Specialty RX, LLC.. 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?
- Chartwell Governmental & Specialty RX, LLC., NDC labeler code 68999. 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.
Related NDCs: other Prednisolone Sodium Phosphate products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| PrednisoLONE Sodium Phosphate | Prednisolone sodium phosphate 5 mg/5mL | SolutionOral | PAI Holdings, LLC dba PAI Pharma | 0121-1100 | 00121-1100-04 |
| Prednisolone Sodium Phosphate | Prednisolone sodium phosphate 15 mg/5mL | SolutionOral | REMEDYREPACK INC. | 70518-4524 | 70518-4524-0070518-4524-0270518-4524-04 |
| Prednisolone Sodium Phosphate | Prednisolone sodium phosphate 15 mg/5mL | SolutionOral | Preferred Pharmaceuticals Inc. | 68788-4046 | 68788-4046-02 |
| Prednisolone Sodium Phosphate | Prednisolone sodium phosphate 15 mg/5mL | SolutionOral | PAI Holdings, LLC dba PAI Pharma | 0121-4759 | 00121-4759-50 |
| Prednisolone Sodium Phosphate | Prednisolone sodium phosphate 15 mg/5mL | SolutionOral | ATLANTIC BIOLOGICALS CORP. | 17856-0815 | 17856-0815-0117856-0815-0217856-0815-03+1 more |
| Prednisolone Sodium Phosphate | Prednisolone sodium phosphate 15 mg/5mL | SolutionOral | Atlantic Biologicals Corp | 17856-8815 | 17856-8815-01 |
| Prednisolone Sodium Phosphate | Prednisolone sodium phosphate 15 mg/5mL | SolutionOral | Edenbridge Pharmaceuticals LLC. | 42799-815 | 42799-0815-01 |
| Prednisolone Sodium Phosphate | Prednisolone sodium phosphate 15 mg/5mL | SolutionOral | Redpharm Drug | 67296-2134 | 67296-2134-06 |
| Prednisolone Sodium Phosphate | Prednisolone sodium phosphate 25 mg/5mL | SolutionOral | Edenbridge Pharmaceuticals LLC. | 42799-816 | 42799-0816-01 |
| Prednisolone Sodium Phosphate | Prednisolone sodium phosphate 15 mg/5mL | SolutionOral | Amneal Pharmaceuticals NY LLC | 69238-2122 | 69238-2122-09 |
Other NDCs under ANDA 075988
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Prednisolone Sodium Phosphate | Prednisolone sodium phosphate 5 mg/5mL | SolutionOral | Chartwell RX, LLC. | 62135-330 |