What is NDC 70710-1158?

70710-1158 is the product NDC for leflunomide, Leflunomide 20 mg/1 tablet, film coated, listed with the FDA by Zydus Pharmaceuticals (USA) Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

Zydus Pharmaceuticals (USA) Inc., NDC labeler code 70710. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for leflunomide?

36 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

leflunomide NDC 70710-1158 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70710-1158Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70710-1158Add 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
70710-1158-1	70710115801	100 TABLET, FILM COATED in 1 BOTTLE (70710-1158-1)Marketed from Apr 26, 2019
70710-1158-3	70710115803	30 TABLET, FILM COATED in 1 BOTTLE (70710-1158-3)Marketed from Apr 26, 2019
70710-1158-5	70710115805	500 TABLET, FILM COATED in 1 BOTTLE (70710-1158-5)Marketed from Apr 26, 2019

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): leflunomide
Generic name (nonproprietary): leflunomide
Active ingredients: Leflunomide — 20 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Zydus Pharmaceuticals (USA) Inc.NDC labeler code 70710
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212308
Marketing start: Apr 26, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 70710-1158_bd138e7f-33f1-44a4-886b-62f5bfbdfe09SPL ID bd138e7f-33f1-44a4-886b-62f5bfbdfe09SPL set ID b9af9870-014f-4c4e-8738-bb04b30b3e85RxCUI 205284, 205285UNII G162GK9U4W
Pharmacologic class: Antirheumatic Agent

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

N470710115801 followed by a unit qualifier and the quantity

Package 70710-1158-01. 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 Aug 12, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

Leflunomide tablets are indicated for the treatment of adults with active rheumatoid arthritis (RA). Leflunomide is a pyrimidine synthesis inhibitor indicated for the treatment of adults with active rheumatoid arthritis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70710-1158

What is NDC 70710-1158?: 70710-1158 is the product NDC for leflunomide, Leflunomide 20 mg/1 tablet, film coated, listed with the FDA by Zydus Pharmaceuticals (USA) Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: leflunomide.
What is the active ingredient?: Leflunomide.
Who is the labeler?: Zydus Pharmaceuticals (USA) Inc., NDC labeler code 70710. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for leflunomide?: 36 other product NDCs are listed under this name. See all leflunomide 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 leflunomide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Leflunomide	Leflunomide 10 mg/1	Tablet, Film coatedOral	Burel Pharmaceuticals, LLC	35573-447	35573-0447-30
Leflunomide	Leflunomide 20 mg/1	Tablet, Film coatedOral	Burel Pharmaceuticals, LLC	35573-448	35573-0448-30
Leflunomide	Leflunomide 20 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-5992	50090-5992-00
Leflunomide	Leflunomide 10 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-348	59651-0348-30
Leflunomide	Leflunomide 20 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-349	59651-0349-30
Leflunomide	Leflunomide 10 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-9728	63629-9728-01
Leflunomide	Leflunomide 20 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2256	71335-2256-0171335-2256-02
Leflunomide	Leflunomide 10 mg/1	TabletOral	AvPAK	50268-477	50268-0477-15
Leflunomide	Leflunomide 20 mg/1	TabletOral	AvPAK	50268-478	50268-0478-15
Leflunomide	Leflunomide 10 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals, Inc.	68071-3763	68071-3763-09

All 37 leflunomide NDCs

Other NDCs under ANDA 212308

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

FDA NDC Directory listings under ANDA 212308
Product	Strength	Form · route	Labeler	Product NDC
leflunomide	Leflunomide 10 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals (USA) Inc.	70710-1157
leflunomide	Leflunomide 20 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2403
leflunomide	Leflunomide 20 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals, Inc.	68071-3764
leflunomide	Leflunomide 10 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1491
leflunomide	Leflunomide 20 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1492
leflunomide	Leflunomide 20 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7537