Ipratropium Bromide Spray, Metered
NDC Package 70748-336-01

11-digit billing NDC: 70748033601 · Billing unit: ML

Package Information

Ipratropium Bromide sprays is ipratropium bromide nasal solution, 0.03% is indicated for the symptomatic relief of rhinorrhea associated with allergic and nonallergic perennial rhinitis in adults and children age 6 years and older. This formulation utilizes a spray, metered delivery system. Marketed by Lupin Pharmaceuticals, Inc., this product is identified by NDC 70748-336 and is authorized under FDA application ANDA217912.

Identification & Billing

NDC Package Code
70748-336-01
Package Description
1 BOTTLE, SPRAY in 1 CARTON / 345 SPRAY, METERED in 1 BOTTLE, SPRAY
Product Code
11-Digit Billing Format
70748033601
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk
  • RxCUI: 1797833 - ipratropium Br 21 MCG/ACTUAT (0.03 % ) Metered Dose Nasal Spray
  • RxCUI: 1797833 - ipratropium bromide 0.021 MG/ACTUAT Metered Dose Nasal Spray
  • RxCUI: 1797833 - ipratropium bromide 21 MCG/ACTUAT Metered Dose Nasal Spray

Clinical Specifications

Proprietary Name
Ipratropium Bromide
Non-Proprietary Name
Ipratropium Bromide
Substance Name
Ipratropium Bromide
Dosage Form
Spray, Metered - A non-pressurized dosage form consisting of valves which allow the dispensing of a specified quantity of spray upon each activation.
Administration Route
Nasal - Administration to the nose; administered by way of the nose.
Active Ingredient(s)
Usage Information
Ipratropium bromide nasal solution, 0.03% is indicated for the symptomatic relief of rhinorrhea associated with allergic and nonallergic perennial rhinitis in adults and children age 6 years and older. Ipratropium bromide 0.03% does not relieve nasal congestion, sneezing, or postnasal drip associated with allergic or nonallergic perennial rhinitis.

Regulatory & Marketing

Labeler Name
Lupin Pharmaceuticals, Inc.
Product Type
Human Prescription Drug
FDA Application #
ANDA217912
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
07-03-2025
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 70748-336-01 identifies a specific commercial package of 1 bottle, spray in 1 carton / 345 spray, metered in 1 bottle, spray of Ipratropium Bromide, a human prescription drug labeled by Lupin Pharmaceuticals, Inc.. This spray, metered is formulated for nasal use and contains ipratropium bromide as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Lupin Pharmaceuticals, Inc. on July 03, 2025. The current certification is valid through December 31, 2027.

How is this Lupin Pharmaceuticals, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70748033601. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
70748-336-01
11-Digit CMS (5-4-2)
70748-0336-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.