Albuterol Sulfate NDC 70518-4496

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4496Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4496Add 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
70518-4496-0	70518449600	1 INHALER in 1 CARTON (70518-4496-0) / 200 INHALANT in 1 INHALERMarketed from Oct 10, 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 — 90 ug/1
Dosage form: Inhalant
Route: Respiratory (Inhalation)
Labeler: REMEDYREPACK INC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212447
Marketing start: Oct 10, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta2-Agonists (Mechanism)
Identifiers: Product ID 70518-4496_5b74442a-d53c-ad42-e063-6294a90a7effSPL ID 5b74442a-d53c-ad42-e063-6294a90a7eff
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

N470518449600 followed by a unit qualifier and the quantity

Package 70518-4496-00. 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 212447

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

FDA NDC Directory listings under ANDA 212447
Product	Strength	Form · route	Labeler	Product NDC
Albuterol Sulfate	Albuterol sulfate 90 ug/1	InhalantRespiratory (Inhalation)	Armstrong Pharmaceuticals, Inc.	17270-0740
Albuterol Sulfate	Albuterol sulfate 90 ug/1	InhalantRespiratory (Inhalation)	NuCare Pharmaceuticals,Inc.	68071-3902
Albuterol Sulfate	Albuterol sulfate 90 ug/1	InhalantRespiratory (Inhalation)	Preferred Pharmaceuticals, Inc.	68788-4041