What is NDC 70771-1923?

70771-1923 is the product NDC for sacubitril and valsartan, Sacubitril 97 mg/1; Valsartan 103 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 3 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 sacubitril and valsartan?

86 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

sacubitril and valsartan NDC 70771-1923

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1923Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1923Add 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
70771-1923-4	70771192304	10 BLISTER PACK in 1 CARTON (70771-1923-4) / 10 TABLET in 1 BLISTER PACK (70771-1923-2)Marketed from Jul 8, 2025
70771-1923-6	70771192306	60 TABLET in 1 BOTTLE (70771-1923-6)Marketed from Jul 8, 2025
70771-1923-8	70771192308	180 TABLET in 1 BOTTLE (70771-1923-8)Marketed from Jul 8, 2025

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): sacubitril and valsartan
Generic name (nonproprietary): sacubitril and valsartan
Active ingredients: Sacubitril — 97 mg/1Valsartan — 103 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 213719
Marketing start: Jul 8, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)Neprilysin Inhibitors (Mechanism)
Identifiers: Product ID 70771-1923_f0d8c298-2823-4537-ae02-c43da2c66e67SPL ID f0d8c298-2823-4537-ae02-c43da2c66e67SPL set ID 4c871c01-0564-411f-87e2-478aa42503cfRxCUI 1656340, 1656349, 1656354UNII 80M03YXJ7I, 17ERJ0MKGI
Pharmacologic class: Angiotensin 2 Receptor Blocker; Neprilysin Inhibitor

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

N470771192304 followed by a unit qualifier and the quantity

Package 70771-1923-04. 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 Jul 8, 2025.

Full label on DailyMed (opens in a new tab)

About NDC 70771-1923

What is NDC 70771-1923?: 70771-1923 is the product NDC for sacubitril and valsartan, Sacubitril 97 mg/1; Valsartan 103 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?: sacubitril and valsartan.
What is the active ingredient?: Sacubitril, Valsartan.
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 sacubitril and valsartan?: 86 other product NDCs are listed under this name. See all sacubitril and valsartan 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 sacubitril and valsartan NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sacubitril and Valsartan	Sacubitril 24 mg/1; Valsartan 26 mg/1	Tablet, Film coatedOral	Umedica Laboratories USA Inc.	60290-085	60290-0085-0160290-0085-0260290-0085-03
Sacubitril and Valsartan	Sacubitril 49 mg/1; Valsartan 51 mg/1	Tablet, Film coatedOral	Umedica Laboratories USA Inc.	60290-086	60290-0086-0160290-0086-0260290-0086-03
Sacubitril and Valsartan	Sacubitril 97 mg/1; Valsartan 103 mg/1	Tablet, Film coatedOral	Umedica Laboratories USA Inc.	60290-087	60290-0087-0160290-0087-0260290-0087-03
Sacubitril and Valsartan	Sacubitril 24 mg/1; Valsartan 26 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-880	72603-0880-0172603-0880-02
Sacubitril and Valsartan	Sacubitril 49 mg/1; Valsartan 51 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-881	72603-0881-0172603-0881-02
Sacubitril and Valsartan	Sacubitril 97 mg/1; Valsartan 103 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-882	72603-0882-0172603-0882-02
sacubitril and valsartan	Sacubitril 24 mg/1; Valsartan 26 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-935	51407-0935-10
sacubitril and valsartan	Sacubitril 49 mg/1; Valsartan 51 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-936	51407-0936-10
sacubitril and valsartan	Sacubitril 97 mg/1; Valsartan 103 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-937	51407-0937-10
Sacubitril and Valsartan	Sacubitril 49 mg/1; Valsartan 51 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-966	60687-0966-57

All 87 sacubitril and valsartan NDCs

Other NDCs under ANDA 213719

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

FDA NDC Directory listings under ANDA 213719
Product	Strength	Form · route	Labeler	Product NDC
sacubitril and valsartan	Sacubitril 24 mg/1; Valsartan 26 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	70710-1272
sacubitril and valsartan	Sacubitril 49 mg/1; Valsartan 51 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	70710-1273
sacubitril and valsartan	Sacubitril 97 mg/1; Valsartan 103 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	70710-1274
sacubitril and valsartan	Sacubitril 24 mg/1; Valsartan 26 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1921
sacubitril and valsartan	Sacubitril 49 mg/1; Valsartan 51 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1922