What is NDC 70771-1351?

70771-1351 is the product NDC for methylprednisolone, Methylprednisolone 32 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 4 package NDCs, shown above in 10- and 11-digit form.

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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

methylprednisolone NDC 70771-1351 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1351Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1351Add 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 NDC	11-digit (billing)	Package
70771-1351-1	7077113510170771135101	100 TABLET in 1 BOTTLE (70771-1351-1)Marketed from May 1, 2018
70771-1351-4	7077113510470771135104	10 BLISTER PACK in 1 CARTON (70771-1351-4) / 10 TABLET in 1 BLISTER PACK (70771-1351-2)Marketed from May 1, 2018
70771-1351-5	7077113510570771135105	500 TABLET in 1 BOTTLE (70771-1351-5)Marketed from May 1, 2018
70771-1351-8	7077113510870771135108	25 TABLET in 1 BOTTLE (70771-1351-8)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 — 32 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: May 1, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 70771-1351_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

N470771135101 followed by a unit qualifier and the quantity

Package 70771-1351-01. 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 Dec 5, 2024.

Full label on DailyMed (opens in a new tab)

About NDC 70771-1351

What is NDC 70771-1351?: 70771-1351 is the product NDC for methylprednisolone, Methylprednisolone 32 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 4 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
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

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
Product	Strength	Form · route	Labeler	Product NDC
methylprednisolone	Methylprednisolone 4 mg/1	TabletOral	Major Pharmaceuticals	0904-6914
methylprednisolone	Methylprednisolone 4 mg/1	TabletOral	A-S Medication Solutions	50090-3811
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	REMEDYREPACK INC.	70518-3622
methylprednisolone	Methylprednisolone 4 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1348
methylprednisolone	Methylprednisolone 8 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1349
methylprednisolone	Methylprednisolone 16 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1350
Methylprednisolone	Methylprednisolone 4 mg/1	TabletOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0231
methylprednisolone	Methylprednisolone 4 mg/1	TabletOral	Proficient Rx LP	82804-007