NDC codes

FDA NDC Directory
Product NDC (as listed)64980-645Labeler and product segments. Claims need a package NDC.
Product NDC at billing width64980-0645Add 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
64980-645-036498006450330 POUCH in 1 CARTON (64980-645-03) / 5 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USEMarketed from Mar 14, 2025
64980-645-066498006450660 POUCH in 1 CARTON (64980-645-06) / 5 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USEMarketed from Mar 14, 2025

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 and Albuterol Sulfate
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)
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 64980-645_56c00e5e-feb7-2a96-e063-6294a90a1825SPL ID 56c00e5e-feb7-2a96-e063-6294a90a1825SPL set ID 3246dfab-61d7-27ba-e063-6294a90ac180RxCUI 1437702UNII J697UZ2A9J, 021SEF3731UPC 0364980645003
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

N464980064503 followed by a unit qualifier and the quantity

Package 64980-0645-03. 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)

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)Preferred Pharmaceuticals Inc.68788-8103
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)Proficient Rx LP71205-051
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)A-S Medication Solutions50090-1669

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