What is NDC 24208-398?

24208-398 is the product NDC for Ipratropium bromide, Ipratropium bromide 21 ug/1 spray, metered, listed with the FDA by Bausch & Lomb Incorporated. It has 1 package NDC, shown above in 10- and 11-digit form.

Bausch & Lomb Incorporated, NDC labeler code 24208. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ipratropium bromide?

32 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ipratropium bromide NDC 24208-398 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)24208-398Labeler and product segments. Claims need a package NDC.

Product NDC at billing width24208-0398Add 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
24208-398-30	24208039830	1 BOTTLE, SPRAY in 1 CARTON (24208-398-30) / 345 SPRAY, METERED in 1 BOTTLE, SPRAYMarketed from Mar 31, 2003

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): Ipratropium bromide
Generic name (nonproprietary): ipratropium bromide
Active ingredients: Ipratropium bromide — 21 ug/1
Dosage form: Spray, Metered
Route: Nasal
Labeler: Bausch & Lomb IncorporatedNDC labeler code 24208
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076025
Marketing start: Mar 31, 2003
Listing expires: Dec 31, 2026
Other FDA classes: Cholinergic Antagonists (Mechanism)
Identifiers: Product ID 24208-398_88d5fb49-7b0f-4d56-be45-8beca99fcd85SPL ID 88d5fb49-7b0f-4d56-be45-8beca99fcd85SPL set ID 1e92b86d-66e1-45e4-9e23-f9310c95bf82RxCUI 1797833UNII J697UZ2A9J
Pharmacologic class: Anticholinergic

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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N424208039830 followed by a unit qualifier and the quantity

Package 24208-0398-30. 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 May 1, 2019.

Indications (excerpt from the label)

INDICATIONS AND USAGE: Ipratropium Bromide Nasal Solution 0.03% (Nasal Spray) 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 Nasal Solution 0.03% (Nasal Spray) does not relieve nasal congestion, sneezing, or postnasal drip associated with allergic or nonallergic perennial rhinitis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 24208-398

What is NDC 24208-398?: 24208-398 is the product NDC for Ipratropium bromide, Ipratropium bromide 21 ug/1 spray, metered, listed with the FDA by Bausch & Lomb Incorporated. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ipratropium bromide.
What is the active ingredient?: Ipratropium bromide.
Who is the labeler?: Bausch & Lomb Incorporated, NDC labeler code 24208. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ipratropium bromide?: 32 other product NDCs are listed under this name. See all Ipratropium bromide NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Ipratropium bromide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ipratropium Bromide	Ipratropium bromide .5 mg/2.5mL	SolutionRespiratory (Inhalation)	Cardinal Health 107, LLC	55154-4411	55154-4411-05
Ipratropium Bromide	Ipratropium bromide 21 ug/1	Spray, MeteredNasal	Lupin Pharmaceuticals, Inc.	70748-336	70748-0336-01
Ipratropium Bromide	Ipratropium bromide 42 ug/1	Spray, MeteredNasal	Lupin Pharmaceuticals, Inc.	70748-337	70748-0337-01
Ipratropium Bromide	Ipratropium bromide 42 ug/1	Spray, MeteredNasal	Sportpharm LLC	85766-242	85766-0242-15
Ipratropium Bromide	Ipratropium bromide 42 ug/1	Spray, MeteredNasal	Oceanside Pharmaceuticals	68682-399	68682-0399-15
Ipratropium Bromide	Ipratropium bromide .5 mg/2.5mL	SolutionRespiratory (Inhalation)	Rising Pharma Holdings, Inc.	64980-640	64980-0640-0264980-0640-0364980-0640-06
Ipratropium Bromide	Ipratropium bromide 21 ug/1	Spray, MeteredNasal	Advagen Pharma Ltd	72888-149	72888-0149-38
Ipratropium Bromide	Ipratropium bromide 42 ug/1	Spray, MeteredNasal	Advagen Pharma Ltd	72888-148	72888-0148-37
Ipratropium Bromide	Ipratropium bromide 21 ug/1	SprayNasal	Amneal Pharmaceuticals NY LLC	69238-2016	69238-2016-03
Ipratropium Bromide	Ipratropium bromide 42 ug/1	SprayNasal	Amneal Pharmaceuticals NY LLC	69238-2017	69238-2017-02

All 33 Ipratropium bromide NDCs

Other NDCs under ANDA 076025

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

FDA NDC Directory listings under ANDA 076025
Product	Strength	Form · route	Labeler	Product NDC
Ipratroprium Bromide	Ipratropium bromide 21 ug/1	Spray, MeteredNasal	Oceanside Pharmaceuticals	68682-398