What is NDC 70518-4528?

70518-4528 is the product NDC for Albuterol Sulfate, Albuterol sulfate 108 ug/1 aerosol, metered, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Albuterol Sulfate?

91 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Albuterol Sulfate NDC 70518-4528 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4528Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4528Add 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
70518-4528-0	7051845280070518452800	1 CANISTER in 1 CARTON (70518-4528-0) / 200 AEROSOL, METERED in 1 CANISTERMarketed from Dec 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 — 108 ug/1
Dosage form: Aerosol, Metered
Route: Respiratory (Inhalation)
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: NDA authorized genericApplication NDA 020503
Marketing start: Dec 3, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta2-Agonists (Mechanism)
Identifiers: Product ID 70518-4528_5b8a4b3d-c84b-d468-e063-6394a90a2571SPL ID 5b8a4b3d-c84b-d468-e063-6394a90a2571
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

N470518452800 followed by a unit qualifier and the quantity

Package 70518-4528-00. 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.

About NDC 70518-4528

What is NDC 70518-4528?: 70518-4528 is the product NDC for Albuterol Sulfate, Albuterol sulfate 108 ug/1 aerosol, metered, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Albuterol Sulfate.
What is the active ingredient?: Albuterol sulfate.
Who is the labeler?: REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Albuterol Sulfate?: 91 other product NDCs are listed under this name. See all Albuterol Sulfate NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Albuterol Sulfate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Albuterol Sulfate	Albuterol sulfate 90 ug/1	InhalantRespiratory (Inhalation)	Preferred Pharmaceuticals, Inc.	68788-4041	68788-4041-02
Albuterol Sulfate	Albuterol sulfate 90 ug/1	InhalantRespiratory (Inhalation)	REMEDYREPACK INC.	70518-4496	70518-4496-00
Albuterol Sulfate	Albuterol sulfate .83 mg/mL	SolutionRespiratory (Inhalation)	REMEDYREPACK INC.	70518-4490	70518-4490-00
Albuterol sulfate	Albuterol sulfate 90 ug/1	Aerosol, MeteredRespiratory (Inhalation)	Preferred Pharmaceuticals, Inc.	68788-8878	68788-8878-02
Albuterol Sulfate	Albuterol sulfate 90 ug/1	InhalantRespiratory (Inhalation)	Preferred Pharmaceuticals Inc.	68788-8874	68788-8874-02
Albuterol Sulfate	Albuterol sulfate 2.5 mg/.5mL	SolutionRespiratory (Inhalation)	Rising Pharma Holdings, Inc.	64980-642	64980-0642-03
Albuterol Sulfate	Albuterol sulfate .63 mg/3mL	SolutionRespiratory (Inhalation)	Rising Pharma Holdings, Inc	64980-643	64980-0643-03
Albuterol Sulfate	Albuterol sulfate 1.25 mg/3mL	SolutionRespiratory (Inhalation)	Rising Pharma Holdings, Inc	64980-644	64980-0644-02
Albuterol Sulfate	Albuterol sulfate 2.5 mg/3mL	SolutionRespiratory (Inhalation)	Rising Pharma Holdings, Inc.	64980-641	64980-0641-0264980-0641-0364980-0641-06
Albuterol Sulfate	Albuterol sulfate 90 ug/1	Aerosol, MeteredRespiratory (Inhalation)	Preferred Pharmaceuticals Inc.	68788-8787	68788-8787-02

All 92 Albuterol Sulfate NDCs

Other NDCs under NDA 020503

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

FDA NDC Directory listings under NDA 020503
Product	Strength	Form · route	Labeler	Product NDC
Albuterol Sulfate	Albuterol sulfate 108 ug/1	Aerosol, MeteredRespiratory (Inhalation)	Sandoz Inc	0781-7296
Albuterol Sulfate	Albuterol sulfate 108 ug/1	Aerosol, MeteredRespiratory (Inhalation)	Preferred Pharmaceuticals Inc.	68788-7996
Albuterol Sulfate	Albuterol sulfate 108 ug/1	Aerosol, MeteredRespiratory (Inhalation)	Proficient Rx LP	82804-036