What is NDC 47335-706?

47335-706 is the product NDC for Ipratropium Bromide, Ipratropium bromide .5 mg/2.5mL solution, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

Sun Pharmaceutical Industries, Inc., NDC labeler code 47335. 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 47335-706 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)47335-706Labeler and product segments. Claims need a package NDC.

Product NDC at billing width47335-0706Add 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
47335-706-49	47335070649	5 POUCH in 1 CARTON (47335-706-49) / 5 VIAL in 1 POUCH (47335-706-48) / 2.5 mL in 1 VIALMarketed from Feb 4, 2020
47335-706-52	47335070652	6 POUCH in 1 CARTON (47335-706-52) / 5 VIAL in 1 POUCH / 2.5 mL in 1 VIALMarketed from Feb 4, 2020
47335-706-54	47335070654	12 POUCH in 1 CARTON (47335-706-54) / 5 VIAL in 1 POUCH / 2.5 mL in 1 VIALMarketed from Feb 4, 2020

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 — .5 mg/2.5mL
Dosage form: Solution
Route: Respiratory (Inhalation)
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 47335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207903
Marketing start: Feb 4, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Cholinergic Antagonists (Mechanism)
Identifiers: Product ID 47335-706_147b55d9-c9f9-4a22-814a-acf834a1864dSPL ID 147b55d9-c9f9-4a22-814a-acf834a1864dSPL set ID 231ae8f2-1ec9-4e0f-90a8-11d7b6222576RxCUI 836358UNII 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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N447335070649 followed by a unit qualifier and the quantity

Package 47335-0706-49. 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 Apr 13, 2022.

Indications (excerpt from the label)

INDICATIONS AND USAGE Ipratropium Bromide Inhalation Solution administered either alone or with other bronchodilators, especially beta adrenergics, is indicated as a bronchodilator for maintenance treatment of bronchospasm associated with chronic obstructive pulmonary disease, including chronic bronchitis and emphysema.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 47335-706

What is NDC 47335-706?: 47335-706 is the product NDC for Ipratropium Bromide, Ipratropium bromide .5 mg/2.5mL solution, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 3 package NDCs, 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?: Sun Pharmaceutical Industries, Inc., NDC labeler code 47335. 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 42 ug/1	Spray, MeteredNasal	Sportpharm LLC	85766-242	85766-0242-15
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	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