NDC codes

FDA NDC Directory
Product NDC (as listed)60687-394Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0394Add 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
60687-394-836068703948330 POUCH in 1 CARTON (60687-394-83) / 1 AMPULE in 1 POUCH (60687-394-79) / 2.5 mL in 1 AMPULEMarketed from Jan 7, 2019

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)
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075693
Marketing start
Listing expires
Other FDA classes
Cholinergic Antagonists (Mechanism)
Identifiers
Product ID 60687-394_1a02e20d-3db7-69da-e063-6294a90aff4bSPL ID 1a02e20d-3db7-69da-e063-6294a90aff4bSPL set ID 8927f392-4c88-4ac1-a934-c444ecf6b2c8RxCUI 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

N460687039483 followed by a unit qualifier and the quantity

Package 60687-0394-83. 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 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)

Other NDCs under ANDA 075693

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

FDA NDC Directory listings under ANDA 075693
ProductStrengthForm · routeLabelerProduct NDC
Ipratropium BromideIpratropium bromide .5 mg/2.5mLSolutionRespiratory (Inhalation)Ritedose Pharmaceuticals, LLC76204-100
Ipratropium BromideIpratropium bromide .5 mg/2.5mLSolutionRespiratory (Inhalation)A-S Medication Solutions50090-6373
Ipratropium BromideIpratropium bromide .5 mg/2.5mLSolutionRespiratory (Inhalation)Mylan Pharmaceuticals Inc.0378-7970
Ipratropium BromideIpratropium bromide .5 mg/2.5mLSolutionRespiratory (Inhalation)A-S Medication Solutions50090-0668
Ipratropium BromideIpratropium bromide .5 mg/2.5mLSolutionRespiratory (Inhalation)Cardinal Health 107, LLC55154-4411
Ipratropium BromideIpratropium bromide .5 mg/2.5mLSolutionRespiratory (Inhalation)Redpharm Drug67296-2246
Ipratropium BromideIpratropium bromide .5 mg/2.5mLSolutionRespiratory (Inhalation)Cardinal Health 107, LLC55154-2134
Ipratropium BromideIpratropium bromide .5 mg/2.5mLSolutionRespiratory (Inhalation)NuCare Pharmaceuticals, Inc.68071-3769

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