Prescription drug · ANDA
methylprednisolone NDC 70771-1350
Methylprednisolone 16 mg/1 · Tablet · Oral · Zydus Lifesciences Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70771-1350-1 | 70771135001 | 100 TABLET in 1 BOTTLE (70771-1350-1)Marketed from May 1, 2018 | |
| 70771-1350-4 | 70771135004 | 10 BLISTER PACK in 1 CARTON (70771-1350-4) / 10 TABLET in 1 BLISTER PACK (70771-1350-2)Marketed from May 1, 2018 | |
| 70771-1350-5 | 70771135005 | 500 TABLET in 1 BOTTLE (70771-1350-5)Marketed from May 1, 2018 | |
| 70771-1350-7 | 70771135007 | 50 TABLET in 1 BOTTLE (70771-1350-7)Marketed from May 1, 2018 |
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)
- methylprednisolone
- Generic name (nonproprietary)
- methylprednisolone
- Active ingredients
- Methylprednisolone — 16 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Zydus Lifesciences Limited
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 206751
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 70771-1350_99239c7c-b107-454a-8cee-9dd6cbd5647bSPL ID 99239c7c-b107-454a-8cee-9dd6cbd5647bSPL set ID fe9c15b5-4264-45f1-87b5-f7e1d6e6ddeeRxCUI 197971, 197973, 259966, 328161UNII X4W7ZR7023UPC 0368382919113
- 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
N470771135001followed by a unit qualifier and the quantityPackage 70771-1350-01. 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 .
Other NDCs under ANDA 206751
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 | Major Pharmaceuticals | 0904-6914 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Advanced Rx Pharmacy of Tennessee, LLC | 80425-0231 |
| methylprednisolone | Methylprednisolone 8 mg/1 | TabletOral | Zydus Lifesciences Limited | 70771-1349 |
| methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Proficient Rx LP | 82804-007 |
| methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Zydus Lifesciences Limited | 70771-1348 |
| methylprednisolone | Methylprednisolone 32 mg/1 | TabletOral | Zydus Lifesciences Limited | 70771-1351 |
| methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | BluePoint Laboratories | 68001-624 |
| methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Zydus Pharmaceuticals USA Inc. | 68382-916 |
| methylprednisolone | Methylprednisolone 8 mg/1 | TabletOral | Zydus Pharmaceuticals USA Inc. | 68382-917 |
| methylprednisolone | Methylprednisolone 16 mg/1 | TabletOral | Zydus Pharmaceuticals USA Inc. | 68382-918 |
| methylprednisolone | Methylprednisolone 32 mg/1 | TabletOral | Zydus Pharmaceuticals USA Inc. | 68382-919 |
| methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | A-S Medication Solutions | 50090-3811 |