Albuterol Sulfate NDC 64980-642

NDC codes

FDA NDC Directory

Product NDC (as listed)64980-642Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64980-0642Add 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
64980-642-03	64980064203	30 POUCH in 1 CARTON (64980-642-03) / 1 VIAL, SINGLE-DOSE in 1 POUCH / .5 mL in 1 VIAL, SINGLE-DOSEMarketed from Apr 30, 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): Albuterol Sulfate
Generic name (nonproprietary): albuterol sulfate
Active ingredients: Albuterol sulfate — 2.5 mg/.5mL
Dosage form: Solution
Route: Respiratory (Inhalation)
Labeler: Rising Pharma Holdings, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075664
Marketing start: Apr 14, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta2-Agonists (Mechanism)
Identifiers: Product ID 64980-642_56c00cc1-5ed0-8ff5-e063-6394a90a132bSPL ID 56c00cc1-5ed0-8ff5-e063-6394a90a132bSPL set ID 3236f82c-14e9-dfd4-e063-6294a90ac43dRxCUI 245314UNII 021SEF3731UPC 0364980642033
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

N464980064203 followed by a unit qualifier and the quantity

Package 64980-0642-03. 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 Jul 16, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Albuterol inhalation solution is indicated for the relief of bronchospasm in patients 12 years of age and older with reversible obstructive airway disease and acute attacks of bronchospasm.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 075664

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

FDA NDC Directory listings under ANDA 075664
Product	Strength	Form · route	Labeler	Product NDC
Albuterol Sulfate	Albuterol sulfate 2.5 mg/.5mL	SolutionRespiratory (Inhalation)	Chartwell RX, LLC.	62135-829
Albuterol Sulfate	Albuterol sulfate 2.5 mg/.5mL	SolutionRespiratory (Inhalation)	Nephron Pharmaceuticals Corporation	0487-9901