NDC codes

FDA NDC Directory
Product NDC (as listed)24208-399Labeler and product segments. Claims need a package NDC.
Product NDC at billing width24208-0399Add 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 NDC11-digit (billing)PackageCopy
24208-399-15242080399151 BOTTLE, SPRAY in 1 CARTON (24208-399-15) / 165 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 — 42 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 076103
Marketing start
Listing expires
Other FDA classes
Cholinergic Antagonists (Mechanism)
Identifiers
Product ID 24208-399_24982952-0064-4ed9-8276-210e482c8358SPL ID 24982952-0064-4ed9-8276-210e482c8358SPL set ID 3fd850a2-af0f-4291-af5d-52c8d6094e64RxCUI 1797844UNII 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

N424208039915 followed by a unit qualifier and the quantity

Package 24208-0399-15. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE: Ipratropium Bromide Nasal Solution 0.06% (Nasal Spray) is indicated for the symptomatic relief of rhinorrhea associated with the common cold or seasonal allergic rhinitis for adults and children age 5 years and older. Ipratropium Bromide Nasal Solution 0.06% (Nasal Spray) does not relieve nasal congestion or sneezing associated with the common cold or seasonal allergic rhinitis. The safety and effectiveness of the use of Ipratropium Bromide Nasal Solution 0.06% (Nasal Spray) beyond four days in patients with the common cold or beyond three weeks in patients with seasonal allergic rhinitis has not been established.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 24208-399

What is NDC 24208-399?
24208-399 is the product NDC for Ipratropium Bromide, Ipratropium bromide 42 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Ipratropium BromideIpratropium bromide .5 mg/2.5mLSolutionRespiratory (Inhalation)Cardinal Health 107, LLC55154-441155154-4411-05
Ipratropium BromideIpratropium bromide 21 ug/1Spray, MeteredNasalLupin Pharmaceuticals, Inc.70748-33670748-0336-01
Ipratropium BromideIpratropium bromide 42 ug/1Spray, MeteredNasalLupin Pharmaceuticals, Inc.70748-33770748-0337-01
Ipratropium BromideIpratropium bromide 42 ug/1Spray, MeteredNasalSportpharm LLC85766-24285766-0242-15
Ipratropium BromideIpratropium bromide 42 ug/1Spray, MeteredNasalOceanside Pharmaceuticals68682-39968682-0399-15
Ipratropium BromideIpratropium bromide .5 mg/2.5mLSolutionRespiratory (Inhalation)Rising Pharma Holdings, Inc.64980-64064980-0640-0264980-0640-0364980-0640-06
Ipratropium BromideIpratropium bromide 21 ug/1Spray, MeteredNasalAdvagen Pharma Ltd72888-14972888-0149-38
Ipratropium BromideIpratropium bromide 42 ug/1Spray, MeteredNasalAdvagen Pharma Ltd72888-14872888-0148-37
Ipratropium BromideIpratropium bromide 21 ug/1SprayNasalAmneal Pharmaceuticals NY LLC69238-201669238-2016-03
Ipratropium BromideIpratropium bromide 42 ug/1SprayNasalAmneal Pharmaceuticals NY LLC69238-201769238-2017-02

All 33 Ipratropium Bromide NDCs

Other NDCs under ANDA 076103

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

FDA NDC Directory listings under ANDA 076103
ProductStrengthForm · routeLabelerProduct NDC
Ipratropium BromideIpratropium bromide 42 ug/1Spray, MeteredNasalOceanside Pharmaceuticals68682-399

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