Prescription drug · ANDA
prednisone NDC 71205-755
Prednisone 50 mg/1 · Tablet · Oral · Proficient Rx LP
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71205-755-05 | 71205075505 | 5 TABLET in 1 BOTTLE (71205-755-05)Marketed from Jan 31, 2023 | |
| 71205-755-06 | 71205075506 | 6 TABLET in 1 BOTTLE (71205-755-06)Marketed from Jan 31, 2023 | |
| 71205-755-07 | 71205075507 | 7 TABLET in 1 BOTTLE (71205-755-07)Marketed from Jan 31, 2023 | |
| 71205-755-10 | 71205075510 | 10 TABLET in 1 BOTTLE (71205-755-10)Marketed from Jan 31, 2023 | |
| 71205-755-12 | 71205075512 | 12 TABLET in 1 BOTTLE (71205-755-12)Marketed from Jan 31, 2023 | |
| 71205-755-14 | 71205075514 | 14 TABLET in 1 BOTTLE (71205-755-14)Marketed from Jan 31, 2023 | |
| 71205-755-15 | 71205075515 | 15 TABLET in 1 BOTTLE (71205-755-15)Marketed from Jan 31, 2023 | |
| 71205-755-18 | 71205075518 | 18 TABLET in 1 BOTTLE (71205-755-18)Marketed from Jan 31, 2023 | |
| 71205-755-20 | 71205075520 | 20 TABLET in 1 BOTTLE (71205-755-20)Marketed from Jan 31, 2023 | |
| 71205-755-21 | 71205075521 | 21 TABLET in 1 BOTTLE (71205-755-21)Marketed from Jan 31, 2023 | |
| 71205-755-24 | 71205075524 | 24 TABLET in 1 BOTTLE (71205-755-24)Marketed from Jan 31, 2023 | |
| 71205-755-28 | 71205075528 | 28 TABLET in 1 BOTTLE (71205-755-28)Marketed from Jan 31, 2023 | |
| 71205-755-30 | 71205075530 | 30 TABLET in 1 BOTTLE (71205-755-30)Marketed from Jan 31, 2023 | |
| 71205-755-60 | 71205075560 | 60 TABLET in 1 BOTTLE (71205-755-60)Marketed from Jan 31, 2023 | |
| 71205-755-90 | 71205075590 | 90 TABLET in 1 BOTTLE (71205-755-90)Marketed from Jan 31, 2023 |
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 — 50 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Proficient Rx LPNDC labeler code 71205
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 208412
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 71205-755_22d9fd96-cad5-4762-9a56-0ff63357ed9eSPL ID 22d9fd96-cad5-4762-9a56-0ff63357ed9eSPL set ID 22d9fd96-cad5-4762-9a56-0ff63357ed9eRxCUI 198148UNII VB0R961HZTUPC 0371205755058
- 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
N471205075505followed by a unit qualifier and the quantityPackage 71205-0755-05. 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 cas…
Excerpt only. Read the full label for complete information.
About NDC 71205-755
- What is NDC 71205-755?
- 71205-755 is the product NDC for prednisone, Prednisone 50 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 15 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?
- Proficient Rx LP, NDC labeler code 71205. 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?
- 282 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 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 |
| prednisone | Prednisone 5 mg/1 | TabletOral | Coupler LLC | 67046-1642 | 67046-1642-03 |
Other NDCs under ANDA 208412
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 | American Health Packaging | 60687-914 |
| Prednisone | Prednisone 20 mg/1 | TabletOral | American Health Packaging | 60687-925 |
| prednisone | Prednisone 20 mg/1 | TabletOral | St. Mary's Medical Park Pharmacy | 60760-790 |
| prednisone | Prednisone 5 mg/1 | TabletOral | Strides Pharma Science Limited | 64380-783 |
| prednisone | Prednisone 10 mg/1 | TabletOral | Strides Pharma Science Limited | 64380-784 |
| prednisone | Prednisone 20 mg/1 | TabletOral | Strides Pharma Science Limited | 64380-785 |
| Prednisone | Prednisone 50 mg/1 | TabletOral | Direct_Rx | 72189-489 |
| prednisone | Prednisone 2.5 mg/1 | TabletOral | Strides Pharma Science Limited | 64380-835 |
| prednisone | Prednisone 20 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-3401 |
| prednisone | Prednisone 10 mg/1 | TabletOral | Proficient Rx LP | 71205-729 |
| prednisone | Prednisone 10 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-3476 |
| prednisone | Prednisone 10 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4038 |
| prednisone | Prednisone 10 mg/1 | TabletOral | A-S Medication Solutions | 50090-7218 |
| prednisone | Prednisone 20 mg/1 | TabletOral | Proficient Rx LP | 71205-741 |
| prednisone | Prednisone 10 mg/1 | TabletOral | A-S Medication Solutions | 50090-7219 |
| prednisone | Prednisone 20 mg/1 | TabletOral | A-S Medication Solutions | 50090-8051 |
| prednisone | Prednisone 20 mg/1 | TabletOral | A-S Medication Solutions | 50090-8052 |
| prednisone | Prednisone 20 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-8663 |
| prednisone | Prednisone 50 mg/1 | TabletOral | Strides Pharma Science Limited | 64380-949 |
| prednisone | Prednisone 5 mg/1 | TabletOral | A-S Medication Solutions | 50090-7505 |
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