Sacubitril and valsartan NDC 31722-675

NDC codes

FDA NDC Directory

Product NDC (as listed)31722-675Labeler and product segments. Claims need a package NDC.

Product NDC at billing width31722-0675Add 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	Copy
31722-675-18	31722067518	180 TABLET, FILM COATED in 1 BOTTLE (31722-675-18)Marketed from Jul 23, 2025
31722-675-60	31722067560	60 TABLET, FILM COATED in 1 BOTTLE (31722-675-60)Marketed from Jul 23, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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, Film coated
Route: Oral
Labeler: Camber Pharmaceuticals, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213668
Marketing start: Jul 23, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)Neprilysin Inhibitors (Mechanism)
Identifiers: Product ID 31722-675_3a93c356-cfa8-4c31-e063-6394a90a536aSPL ID 3a93c356-cfa8-4c31-e063-6394a90a536aSPL set ID 65a3e298-279d-4498-a7be-5f9ee5bc77d8RxCUI 1656340, 1656349, 1656354UNII 80M03YXJ7I, 17ERJ0MKGIUPC 0331722673600, 0331722675604, 0331722674607
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

N431722067518 followed by a unit qualifier and the quantity

Package 31722-0675-18. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 213668

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

FDA NDC Directory listings under ANDA 213668
Product	Strength	Form · route	Labeler	Product NDC
Sacubitril and valsartan	Sacubitril 24 mg/1; Valsartan 26 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-673
Sacubitril and valsartan	Sacubitril 49 mg/1; Valsartan 51 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-674