Fosinopril sodium NDC 71335-9703

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-9703Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-9703Add 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
71335-9703-1	71335970301	30 TABLET in 1 BOTTLE (71335-9703-1)Marketed from May 11, 2023
71335-9703-2	71335970302	90 TABLET in 1 BOTTLE (71335-9703-2)Marketed from May 11, 2023
71335-9703-3	71335970303	28 TABLET in 1 BOTTLE (71335-9703-3)Marketed from May 11, 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): Fosinopril sodium
Generic name (nonproprietary): fosinopril sodium
Active ingredients: Fosinopril sodium — 40 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch Prepack
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205670
Marketing start: Oct 1, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)
Identifiers: Product ID 71335-9703_c526a852-6b47-4687-b543-f63e7aaf67e7SPL ID c526a852-6b47-4687-b543-f63e7aaf67e7SPL set ID ee78de8e-22f4-4c3b-a721-e9464d704edaRxCUI 857187UNII NW2RTH6T2N
Pharmacologic class: Angiotensin Converting Enzyme 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

N471335970301 followed by a unit qualifier and the quantity

Package 71335-9703-01. 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

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

Other NDCs under ANDA 205670

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

FDA NDC Directory listings under ANDA 205670
Product	Strength	Form · route	Labeler	Product NDC
Fosinopril sodium	Fosinopril sodium 40 mg/1	TabletOral	A-S Medication Solutions	50090-4743
Fosinopril sodiumfosinopirl sodium	Fosinopril sodium 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-0726
Fosinopril sodiumfosinopirl sodium	Fosinopril sodium 10 mg/1	TabletOral	Solco Healthcare LLC	43547-386
Fosinopril sodium	Fosinopril sodium 20 mg/1	TabletOral	Solco Healthcare LLC	43547-387
Fosinopril sodium	Fosinopril sodium 40 mg/1	TabletOral	Solco Healthcare LLC	43547-388