What is NDC 70771-1737?

70771-1737 is the product NDC for Lurasidone hydrochloride, Lurasidone hydrochloride 80 mg/1 tablet, coated, listed with the FDA by Zydus Lifesciences Limited. It has 5 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 Lurasidone hydrochloride?

127 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Lurasidone hydrochloride NDC 70771-1737

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1737Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1737Add 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
70771-1737-1	70771173701	100 TABLET, COATED in 1 BOTTLE (70771-1737-1)Marketed from Feb 1, 2023
70771-1737-3	70771173703	30 TABLET, COATED in 1 BOTTLE (70771-1737-3)Marketed from Feb 1, 2023
70771-1737-4	70771173704	10 BLISTER PACK in 1 CARTON (70771-1737-4) / 10 TABLET, COATED in 1 BLISTER PACK (70771-1737-2)Marketed from Feb 1, 2023
70771-1737-5	70771173705	500 TABLET, COATED in 1 BOTTLE (70771-1737-5)Marketed from Feb 1, 2023
70771-1737-9	70771173709	90 TABLET, COATED in 1 BOTTLE (70771-1737-9)Marketed from Feb 1, 2023

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): Lurasidone hydrochloride
Generic name (nonproprietary): lurasidone hydrochloride
Active ingredients: Lurasidone hydrochloride — 80 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208052
Marketing start: Feb 1, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 70771-1737_b82674a0-84e9-4431-9041-e5c360bbdacaSPL ID b82674a0-84e9-4431-9041-e5c360bbdacaSPL set ID 0f5f8228-1304-4981-8577-029136627260RxCUI 1040031, 1040041, 1235247, 1297278, 1431235UNII O0P4I5851I
Pharmacologic class: Atypical Antipsychotic

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

N470771173701 followed by a unit qualifier and the quantity

Package 70771-1737-01. 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 Nov 30, 2024.

Full label on DailyMed (opens in a new tab)

About NDC 70771-1737

What is NDC 70771-1737?: 70771-1737 is the product NDC for Lurasidone hydrochloride, Lurasidone hydrochloride 80 mg/1 tablet, coated, listed with the FDA by Zydus Lifesciences Limited. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Lurasidone hydrochloride.
What is the active ingredient?: Lurasidone hydrochloride.
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 Lurasidone hydrochloride?: 127 other product NDCs are listed under this name. See all Lurasidone hydrochloride 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 Lurasidone hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Lurasidone Hydrochloride	Lurasidone hydrochloride 60 mg/1	Tablet, Film coatedOral	Torrent Pharmaceuticals Limited	13668-737	13668-0737-3013668-0737-90
Lurasidone Hydrochloride	Lurasidone hydrochloride 60 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1659	67046-1659-03
Lurasidone Hydrochloride	Lurasidone hydrochloride 20 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4563	70518-4563-00
Lurasidone Hydrochloride	Lurasidone hydrochloride 60 mg/1	TabletOral	Coupler LLC	67046-1654	67046-1654-03
Lurasidone Hydrochloride	Lurasidone hydrochloride 40 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1637	67046-1637-03
Lurasidone Hydrochloride	Lurasidone hydrochloride 40 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4491	70518-4491-00
lurasidone hydrochloride	Lurasidone hydrochloride 40 mg/1	TabletOral	REMEDYREPACK INC.	70518-4427	70518-4427-00
lurasidone hydrochloride	Lurasidone hydrochloride 20 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-621	72603-0621-01
lurasidone hydrochloride	Lurasidone hydrochloride 40 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-622	72603-0622-01
lurasidone hydrochloride	Lurasidone hydrochloride 60 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-623	72603-0623-01

All 128 Lurasidone hydrochloride NDCs

Other NDCs under ANDA 208052

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

FDA NDC Directory listings under ANDA 208052
Product	Strength	Form · route	Labeler	Product NDC
Lurasidone hydrochloride	Lurasidone hydrochloride 60 mg/1	Tablet, CoatedOral	Zydus Pharmaceuticals USA Inc.	68382-859
Lurasidone hydrochloride	Lurasidone hydrochloride 20 mg/1	Tablet, CoatedOral	Zydus Pharmaceuticals USA Inc.	68382-965
Lurasidone hydrochloride	Lurasidone hydrochloride 40 mg/1	Tablet, CoatedOral	Zydus Pharmaceuticals USA Inc.	68382-966
Lurasidone hydrochloride	Lurasidone hydrochloride 80 mg/1	Tablet, CoatedOral	Zydus Pharmaceuticals USA Inc.	68382-967
Lurasidone hydrochloride	Lurasidone hydrochloride 120 mg/1	Tablet, CoatedOral	Zydus Pharmaceuticals USA Inc.	68382-968
Lurasidone hydrochloride	Lurasidone hydrochloride 20 mg/1	Tablet, CoatedOral	Zydus Lifesciences Limited	70771-1734
Lurasidone hydrochloride	Lurasidone hydrochloride 40 mg/1	Tablet, CoatedOral	Zydus Lifesciences Limited	70771-1735
Lurasidone hydrochloride	Lurasidone hydrochloride 60 mg/1	Tablet, CoatedOral	Zydus Lifesciences Limited	70771-1736
Lurasidone hydrochloride	Lurasidone hydrochloride 120 mg/1	Tablet, CoatedOral	Zydus Lifesciences Limited	70771-1738