NDC Package 70069-829-01 Nitrofurantoin

For Suspension Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
70069-829-01
Package Description:
1 BOTTLE, GLASS in 1 CARTON / 230 mL in 1 BOTTLE, GLASS
Product Code:
Proprietary Name:
Nitrofurantoin
Non-Proprietary Name:
Nitrofurantoin
Substance Name:
Nitrofurantoin
Usage Information:
Nitrofurantoin is an antibiotic used to treat or prevent certain bladder infections. It works by stopping the growth of bacteria. This antibiotic treats only bacterial infections. It will not work for viral infections (such as common cold, flu). Using any antibiotic when it is not needed can cause it to not work for future infections. This medication should not be used in infants younger than 1 month old (see also Precautions section). This drug should not be used to treat infections outside the bladder (including kidney infections such as pyelonephritis or perinephric abscesses).
11-Digit NDC Billing Format:
70069082901
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Somerset Therapeutics, Llc
Dosage Form:
For Suspension - A product, usually a solid, intended for suspension prior to administration.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Sample Package:
No
FDA Application Number:
ANDA208909
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
02-26-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

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Frequently Asked Questions

What is NDC 70069-829-01?

The NDC Packaged Code 70069-829-01 is assigned to a package of 1 bottle, glass in 1 carton / 230 ml in 1 bottle, glass of Nitrofurantoin, a human prescription drug labeled by Somerset Therapeutics, Llc. The product's dosage form is for suspension and is administered via oral form.

Is NDC 70069-829 included in the NDC Directory?

Yes, Nitrofurantoin with product code 70069-829 is active and included in the NDC Directory. The product was first marketed by Somerset Therapeutics, Llc on February 26, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 70069-829-01?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 70069-829-01?

The 11-digit format is 70069082901. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-270069-829-015-4-270069-0829-01