Albuterol Sulfate NDC 59651-183

NDC codes

FDA NDC Directory

Product NDC (as listed)59651-183Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59651-0183Add 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	Copy
59651-183-25	59651018325	5 POUCH in 1 CARTON (59651-183-25) / 5 VIAL in 1 POUCH / 3 mL in 1 VIALMarketed from Apr 20, 2020
59651-183-30	59651018330	6 POUCH in 1 CARTON (59651-183-30) / 5 VIAL in 1 POUCH / 3 mL in 1 VIALMarketed from Jul 29, 2024

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): Albuterol Sulfate
Generic name (nonproprietary): albuterol sulfate
Active ingredients: Albuterol sulfate — .63 mg/3mL
Dosage form: Solution
Route: Respiratory (Inhalation)
Labeler: Aurobindo Pharma Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211888
Marketing start: Apr 20, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta2-Agonists (Mechanism)
Identifiers: Product ID 59651-183_1e853c87-b534-65d2-e063-6394a90a7923SPL ID 1e853c87-b534-65d2-e063-6394a90a7923SPL set ID 78e6bee2-7113-46cf-8c97-dc61b0f7b94fRxCUI 351136, 351137UNII 021SEF3731UPC 0359651183052, 0359651184059
Pharmacologic class: 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

N459651018325 followed by a unit qualifier and the quantity

Package 59651-0183-25. 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 Jul 31, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Albuterol sulfate inhalation solution is indicated for the relief of bronchospasm in patients 2 to 12 years of age with asthma (reversible obstructive airway disease).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 211888

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

FDA NDC Directory listings under ANDA 211888
Product	Strength	Form · route	Labeler	Product NDC
Albuterol Sulfate	Albuterol sulfate .63 mg/3mL	SolutionRespiratory (Inhalation)	Luoxin Aurovitas Pharma (Chengdu) Co., Ltd.	81894-105
Albuterol Sulfate	Albuterol sulfate 1.25 mg/3mL	SolutionRespiratory (Inhalation)	Luoxin Aurovitas Pharma (Chengdu) Co., Ltd.	81894-106
Albuterol Sulfate	Albuterol sulfate 1.25 mg/3mL	SolutionRespiratory (Inhalation)	Aurobindo Pharma Limited	59651-184