NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1348Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1348Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
70771-1348-17077113480170771134801100 TABLET in 1 BOTTLE (70771-1348-1)Marketed from May 1, 2018
70771-1348-370771134803707711348031 BLISTER PACK in 1 CARTON (70771-1348-3) / 21 TABLET in 1 BLISTER PACKMarketed from May 1, 2018
70771-1348-57077113480570771134805500 TABLET in 1 BOTTLE (70771-1348-5)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 — 4 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Zydus Lifesciences LimitedNDC labeler code 70771
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 70771-1348_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

N470771134801 followed by a unit qualifier and the quantity

Package 70771-1348-01. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 70771-1348

What is NDC 70771-1348?
70771-1348 is the product NDC for methylprednisolone, Methylprednisolone 4 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 3 package NDCs, 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?
Zydus Lifesciences Limited, NDC labeler code 70771. 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.

Other finished products listed under the same name: strengths, forms and labelers.

Other methylprednisolone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
methylprednisoloneMethylprednisolone 4 mg/1TabletOralBluePoint Laboratories68001-62468001-0624-01
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralREMEDYREPACK INC.70518-421370518-4213-00
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-96160760-0961-21
methylprednisoloneMethylprednisolone 4 mg/1TabletOralREMEDYREPACK INC.70518-362270518-3622-01
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-023080425-0230-01
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-023180425-0231-01
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-025580425-0255-01
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralDirect_Rx72189-26472189-0264-21
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-783368788-7833-02
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralREMEDYREPACK INC.70518-286470518-2864-00

All 49 methylprednisolone NDCs

Other NDCs under ANDA 206751

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 206751
ProductStrengthForm · routeLabelerProduct NDC
methylprednisoloneMethylprednisolone 4 mg/1TabletOralMajor Pharmaceuticals0904-6914
methylprednisoloneMethylprednisolone 4 mg/1TabletOralA-S Medication Solutions50090-3811
methylprednisoloneMethylprednisolone 4 mg/1TabletOralBluePoint Laboratories68001-624
methylprednisoloneMethylprednisolone 4 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-916
methylprednisoloneMethylprednisolone 8 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-917
methylprednisoloneMethylprednisolone 16 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-918
methylprednisoloneMethylprednisolone 32 mg/1TabletOralZydus Pharmaceuticals USA Inc.68382-919
methylprednisoloneMethylprednisolone 4 mg/1TabletOralREMEDYREPACK INC.70518-3622
methylprednisoloneMethylprednisolone 8 mg/1TabletOralZydus Lifesciences Limited70771-1349
methylprednisoloneMethylprednisolone 16 mg/1TabletOralZydus Lifesciences Limited70771-1350
methylprednisoloneMethylprednisolone 32 mg/1TabletOralZydus Lifesciences Limited70771-1351
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0231
methylprednisoloneMethylprednisolone 4 mg/1TabletOralProficient Rx LP82804-007

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