Albuterol Sulfate NDC 70518-4490

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4490Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4490Add 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
70518-4490-0	70518449000	5 POUCH in 1 CARTON (70518-4490-0) / 5 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSEMarketed from Oct 3, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — .83 mg/mL
Dosage form: Solution
Route: Respiratory (Inhalation)
Labeler: REMEDYREPACK INC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206224
Marketing start: Oct 3, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta2-Agonists (Mechanism)
Identifiers: Product ID 70518-4490_5b875db4-187b-4393-e063-6294a90ad895SPL ID 5b875db4-187b-4393-e063-6294a90ad895
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

N470518449000 followed by a unit qualifier and the quantity

Package 70518-4490-00. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 206224

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

FDA NDC Directory listings under ANDA 206224
Product	Strength	Form · route	Labeler	Product NDC
Albuterol Sulfate	Albuterol sulfate .83 mg/mL	SolutionRespiratory (Inhalation)	Luoxin Aurovitas Pharma (Chengdu) Co., Ltd.	81894-104
Albuterol Sulfate	Albuterol sulfate .83 mg/mL	SolutionRespiratory (Inhalation)	Aurobindo Pharma Limited	65862-858