NDC codes

FDA NDC Directory
Product NDC (as listed)71205-051Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0051Add 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
71205-051-0571205005105712050051055 POUCH in 1 CARTON (71205-051-05) / 1 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USEMarketed from Jan 10, 2024
71205-051-15712050051157120500511515 POUCH in 1 CARTON (71205-051-15) / 1 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USEMarketed from Apr 1, 2019
71205-051-30712050051307120500513030 POUCH in 1 CARTON (71205-051-30) / 1 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USEMarketed from Jun 1, 2018

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

Generic name (nonproprietary)
ipratropium bromide and albuterol sulfate
Active ingredients
Ipratropium bromide — .5 mg/3mLAlbuterol sulfate — 3 mg/3mL
Dosage form
Solution
Route
Respiratory (Inhalation)
Labeler
Proficient Rx LPNDC labeler code 71205
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076749
Marketing start
Listing expires
Other FDA classes
Adrenergic beta2-Agonists (Mechanism)Cholinergic Antagonists (Mechanism)
Identifiers
Product ID 71205-051_eba3cb7b-c393-4fc7-84ae-ee1b0d1ef90dSPL ID eba3cb7b-c393-4fc7-84ae-ee1b0d1ef90dSPL set ID a1d9d346-91a5-4f5a-82ed-4ebeaf350a06RxCUI 1437702UNII J697UZ2A9J, 021SEF3731UPC 0371205051051
Pharmacologic class
Anticholinergic; beta2-Adrenergic Agonist

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

N471205005105 followed by a unit qualifier and the quantity

Package 71205-0051-05. 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 and Albuterol Sulfate Inhalation Solution is indicated for the treatment of bronchospasm associated with COPD in patients requiring more than one bronchodilator.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-051

What is NDC 71205-051?
71205-051 is the product NDC for Ipratropium Bromide and Albuterol Sulfate, Ipratropium bromide .5 mg/3mL; Albuterol sulfate 3 mg/3mL solution, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ipratropium Bromide and Albuterol Sulfate.
What is the active ingredient?
Ipratropium bromide, Albuterol sulfate.
Who is the labeler?
Proficient Rx LP, NDC labeler code 71205. 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 and Albuterol Sulfate?
16 other product NDCs are listed under this name. See all Ipratropium Bromide and Albuterol Sulfate 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 and Albuterol Sulfate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Ipratropium Bromide and Albuterol SulfateIpratropium bromide .5 mg/3mL; Albuterol sulfate 3 mg/3mLSolutionRespiratory (Inhalation)Rising Pharma Holdings, Inc.64980-64564980-0645-0364980-0645-06
Ipratropium Bromide and Albuterol SulfateIpratropium bromide .5 mg/3mL; Albuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Sun Pharmaceutical Industries, Inc.47335-75647335-0756-4947335-0756-52
Ipratropium Bromide and Albuterol SulfateIpratropium bromide .5 mg/3mL; Albuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Proficient Rx LP71205-72671205-0726-15
Ipratropium Bromide and Albuterol SulfateIpratropium bromide .5 mg/3mL; Albuterol sulfate 3 mg/3mLSolutionRespiratory (Inhalation)Preferred Pharmaceuticals Inc.68788-810368788-8103-03
Ipratropium Bromide and Albuterol SulfateAlbuterol sulfate 2.5 mg/3mL; Ipratropium bromide .5 mg/3mLSolutionRespiratory (Inhalation)Aurobindo Pharma Limited65862-90665862-0906-0365862-0906-3065862-0906-60
Ipratropium Bromide and Albuterol SulfateIpratropium bromide .5 mg/3mL; Albuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Cipla USA Inc.69097-84069097-0840-5369097-0840-6469097-0840-87
Ipratropium Bromide And Albuterol SulfateAlbuterol sulfate 2.5 mg/3mL; Ipratropium bromide .5 mg/3mLSolutionRespiratory (Inhalation)American Health Packaging60687-40560687-0405-83
Ipratropium Bromide and Albuterol SulfateIpratropium bromide .5 mg/3mL; Albuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Mylan Pharmaceuticals Inc.0378-967100378-9671-3000378-9671-6000378-9671-93
Ipratropium Bromide And Albuterol SulfateAlbuterol sulfate 2.5 mg/3mL; Ipratropium bromide .5 mg/3mLSolutionRespiratory (Inhalation)A-S Medication Solutions50090-138250090-1382-00
Ipratropium Bromide And Albuterol SulfateAlbuterol sulfate 2.5 mg/3mL; Ipratropium bromide .5 mg/3mLSolutionRespiratory (Inhalation)Redpharm Drug67296-231567296-2315-09

All 17 Ipratropium Bromide and Albuterol Sulfate NDCs

Other NDCs under ANDA 076749

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

FDA NDC Directory listings under ANDA 076749
ProductStrengthForm · routeLabelerProduct NDC
Ipratropium Bromide and Albuterol SulfateIpratropium bromide .5 mg/3mL; Albuterol sulfate 3 mg/3mLSolutionRespiratory (Inhalation)Nephron Pharmaceuticals Corporation0487-0201
Ipratropium Bromide and Albuterol SulfateIpratropium bromide .5 mg/3mL; Albuterol sulfate 3 mg/3mLSolutionRespiratory (Inhalation)A-S Medication Solutions50090-1669
Ipratropium Bromide and Albuterol SulfateIpratropium bromide .5 mg/3mL; Albuterol sulfate 3 mg/3mLSolutionRespiratory (Inhalation)Chartwell RX, LLC62135-831
Ipratropium Bromide and Albuterol SulfateIpratropium bromide .5 mg/3mL; Albuterol sulfate 3 mg/3mLSolutionRespiratory (Inhalation)Rising Pharma Holdings, Inc.64980-645
Ipratropium Bromide and Albuterol SulfateIpratropium bromide .5 mg/3mL; Albuterol sulfate 3 mg/3mLSolutionRespiratory (Inhalation)Preferred Pharmaceuticals Inc.68788-8103

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