Methenamine hippurate NDC 70771-1919

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1919Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1919Add 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
70771-1919-1	70771191901	100 TABLET in 1 BOTTLE (70771-1919-1)Marketed from Mar 12, 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): Methenamine hippurate
Generic name (nonproprietary): methenamine hippurate
Active ingredients: Methenamine hippurate — 1 g/1
Dosage form: Tablet
Route: Oral
Labeler: Zydus Lifesciences Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219661
Marketing start: Mar 12, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 70771-1919_c3524692-fabc-438a-9d6e-2cca27172693SPL ID c3524692-fabc-438a-9d6e-2cca27172693SPL set ID 7e0d13d1-e564-4f3e-9054-65161eddfc57RxCUI 992150UNII M329791L57

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

N470771191901 followed by a unit qualifier and the quantity

Package 70771-1919-01. 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 Mar 12, 2025.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 219661

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

FDA NDC Directory listings under ANDA 219661
Product	Strength	Form · route	Labeler	Product NDC
Methenamine hippurate	Methenamine hippurate 1 g/1	TabletOral	Viona Pharmaceuticals Inc	72578-175