Prescription drug · ANDA
Methylprednisolone NDC 76420-041
Methylprednisolone 4 mg/1 · Tablet · Oral · Asclemed USA, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 76420-041-21 | 7642000412176420004121 | 21 TABLET in 1 BLISTER PACK (76420-041-21)Marketed from Jan 23, 2020 |
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)
- Methylprednisolone
- Generic name (nonproprietary)
- methylprednisolone
- Active ingredients
- Methylprednisolone — 4 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Asclemed USA, Inc.NDC labeler code 76420
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 040189
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 76420-041_ead14e8e-059c-1ebb-e053-2995a90a78b3SPL ID ead14e8e-059c-1ebb-e053-2995a90a78b3SPL set ID 8bfdc471-54f7-4298-ba2f-e5c1f6c48456RxCUI 259966, 762675UNII X4W7ZR7023
- 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
N476420004121followed by a unit qualifier and the quantityPackage 76420-0041-21. 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 Methylprednisolone Tablets are indicated in the following conditions: 1.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 Nonsuppurative thyroiditis Hypercalcemia associated with cancer 2.Rheumatic Disorders As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in: Rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require l…
Excerpt only. Read the full label for complete information.
About NDC 76420-041
- What is NDC 76420-041?
- 76420-041 is the product NDC for Methylprednisolone, Methylprednisolone 4 mg/1 tablet, listed with the FDA by Asclemed USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Methylprednisolone.
- What is the active ingredient?
- Methylprednisolone.
- Who is the labeler?
- Asclemed USA, Inc., NDC labeler code 76420. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Methylprednisolone?
- 48 other product NDCs are listed under this name. See all Methylprednisolone NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Methylprednisolone products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | BluePoint Laboratories | 68001-624 | 68001-0624-01 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4213 | 70518-4213-00 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | St. Mary's Medical Park Pharmacy | 60760-961 | 60760-0961-21 |
| methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-3622 | 70518-3622-01 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Advanced Rx Pharmacy of Tennessee, LLC | 80425-0230 | 80425-0230-01 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Advanced Rx Pharmacy of Tennessee, LLC | 80425-0231 | 80425-0231-01 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Advanced Rx Pharmacy of Tennessee, LLC | 80425-0255 | 80425-0255-01 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Direct_Rx | 72189-264 | 72189-0264-21 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-7833 | 68788-7833-02 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-2864 | 70518-2864-00 |
Other NDCs under ANDA 040189
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 |
|---|---|---|---|---|
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | A-S Medication Solutions | 50090-3094 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Proficient Rx LP | 63187-160 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Advanced Rx Pharmacy of Tennessee, LLC | 80425-0230 |