Prescription drug · ANDA
Prednisone NDC 51655-410
Prednisone 10 mg/1 · Tablet · Oral · Northwind Health Company, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 51655-410-20 | 5165504102051655041020 | 20 TABLET in 1 BOTTLE (51655-410-20)Marketed from Apr 28, 2014 | |
| 51655-410-21 | 5165504102151655041021 | 21 TABLET in 1 BOTTLE, PLASTIC (51655-410-21)Marketed from Jun 10, 2021 | |
| 51655-410-27 | 5165504102751655041027 | 12 TABLET in 1 BOTTLE, PLASTIC (51655-410-27)Marketed from Mar 3, 2023 | |
| 51655-410-49 | 5165504104951655041049 | 42 TABLET in 1 BOTTLE (51655-410-49)Marketed from Apr 28, 2014 | |
| 51655-410-52 | 5165504105251655041052 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-410-52)Marketed from Apr 10, 2020 | |
| 51655-410-53 | 5165504105351655041053 | 10 TABLET in 1 BOTTLE, PLASTIC (51655-410-53)Marketed from Mar 15, 2023 | |
| 51655-410-54 | 5165504105451655041054 | 15 TABLET in 1 BOTTLE, PLASTIC (51655-410-54)Marketed from May 12, 2021 |
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)
- Prednisone
- Generic name (nonproprietary)
- prednisone
- Active ingredients
- Prednisone — 10 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Northwind Health Company, LLCNDC labeler code 51655
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 085162
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 51655-410_48ff0341-60c9-05c3-e063-6294a90a031bSPL ID 48ff0341-60c9-05c3-e063-6294a90a031bSPL set ID 0f377d9f-b2f4-4dae-b503-5f963bea281fRxCUI 198145UNII VB0R961HZT
- 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
N451655041020followed by a unit qualifier and the quantityPackage 51655-0410-20. 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 Prednisone tablets, USP are indicated in the following conditions: Endocrine Disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance); congenital adrenal hyperplasia; hypercalcemia associated with cancer; nonsuppurative thyroiditis. Rheumatic Disorders As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in: psoriatic arthritis, rheumatoid arthritis, including juvenile rheumatoid arthritis (selected ca…
Excerpt only. Read the full label for complete information.
About NDC 51655-410
- What is NDC 51655-410?
- 51655-410 is the product NDC for Prednisone, Prednisone 10 mg/1 tablet, listed with the FDA by Northwind Health Company, LLC. It has 7 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Prednisone.
- What is the active ingredient?
- Prednisone.
- Who is the labeler?
- Northwind Health Company, LLC, NDC labeler code 51655. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Prednisone?
- 281 other product NDCs are listed under this name. See all Prednisone NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Prednisone products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| PredniSONE | Prednisone 10 mg/1 | TabletOral | Coupler LLC | 67046-1294 | 67046-1294-03 |
| PredniSONE | Prednisone 20 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-4182 | 68788-4182-0168788-4182-0268788-4182-03+3 more |
| prednisone | Prednisone 10 mg/1 | TabletOral | Unit Dose Solutions, Inc. | 87441-069 | 87441-0069-01 |
| prednisone | Prednisone 50 mg/1 | TabletOral | Coupler LLC | 67046-1171 | 67046-1171-03 |
| prednisone | Prednisone 5 mg/1 | TabletOral | Cardinal Health 107, LLC | 55154-2582 | 55154-2582-00 |
| prednisone | Prednisone 10 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4660 | 70518-4660-00 |
| Prednisone | Prednisone 50 mg/1 | TabletOral | Coupler LLC | 67046-1379 | 67046-1379-03 |
| Prednisone | Prednisone 20 mg/1 | TabletOral | Cardinal Health 107, LLC | 55154-2581 | 55154-2581-00 |
| Prednisone | Prednisone 10 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4560 | 70518-4560-00 |
| prednisone | Prednisone 5 mg/1 | TabletOral | American Health Packaging | 60687-903 | 60687-0903-01 |
Other NDCs under ANDA 085162
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 |
|---|---|---|---|---|
| Prednisone | Prednisone 10 mg/1 | TabletOral | QPharma, Inc. | 42708-115 |
| Prednisone | Prednisone 10 mg/1 | TabletOral | Redpharm Drug | 67296-0140 |
| Prednisone | Prednisone 10 mg/1 | TabletOral | Proficient Rx LP | 71205-362 |
| Prednisone | Prednisone 10 mg/1 | TabletOral | Advanced Rx of Tennessee, LLC | 80425-0491 |
| Prednisone D/P | Prednisone 10 mg/1 | TabletOral | Direct_Rx | 72189-646 |