What is NDC 72162-2064?

72162-2064 is the product NDC for Albuterol Sulfate, Albuterol sulfate 2 mg/5mL syrup, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 72162. 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 72162-2064 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-2064Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-2064Add 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
72162-2064-2	7216220640272162206402	473 mL in 1 BOTTLE (72162-2064-2)Marketed from Aug 15, 2023

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 — 2 mg/5mL
Dosage form: Syrup
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 72162
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212197
Marketing start: Sep 6, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta2-Agonists (Mechanism)
Identifiers: Product ID 72162-2064_04fd53e4-2877-4738-b62b-527b3770ba4cSPL ID 04fd53e4-2877-4738-b62b-527b3770ba4cSPL set ID 45e07bdd-78f9-4055-9de3-646e67de7eafRxCUI 755497UNII 021SEF3731
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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N472162206402 followed by a unit qualifier and the quantity

Package 72162-2064-02. 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 Aug 15, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Albuterol Sulfate Syrup is indicated for the relief of bronchospasm in adults and children 2 years of age and older with reversible obstructive airway disease.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2064

What is NDC 72162-2064?: 72162-2064 is the product NDC for Albuterol Sulfate, Albuterol sulfate 2 mg/5mL syrup, listed with the FDA by Bryant Ranch Prepack. 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?: Bryant Ranch Prepack, NDC labeler code 72162. 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 108 ug/1	Aerosol, MeteredRespiratory (Inhalation)	REMEDYREPACK INC.	70518-4528	70518-4528-00
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

All 92 Albuterol Sulfate NDCs

Other NDCs under ANDA 212197

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

FDA NDC Directory listings under ANDA 212197
Product	Strength	Form · route	Labeler	Product NDC
Albuterol Sulfate	Albuterol sulfate 2 mg/5mL	SyrupOral	Preferred Pharmaceuticals, Inc.	68788-7573
Albuterol Sulfate	Albuterol sulfate 2 mg/5mL	SyrupOral	QUAGEN PHARMACEUTICALS LLC	70752-102
Albuterol Sulfate	Albuterol sulfate 2 mg/5mL	SyrupOral	Bryant Ranch Prepack	71335-2907