Albuterol Sulfate NDC 68788-7573

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-7573Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-7573Add 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
68788-7573-4	68788757304	473 mL in 1 BOTTLE (68788-7573-4)Marketed from May 1, 2020

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: Preferred Pharmaceuticals, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212197
Marketing start: May 1, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta2-Agonists (Mechanism)
Identifiers: Product ID 68788-7573_e9b207d7-0c31-45ac-a0ab-8d5b96ffd983SPL ID e9b207d7-0c31-45ac-a0ab-8d5b96ffd983SPL set ID 4aafc2dd-744d-4726-828f-70355aee6f70RxCUI 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

N468788757304 followed by a unit qualifier and the quantity

Package 68788-7573-04. 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 Jan 3, 2025.

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)

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	QUAGEN PHARMACEUTICALS LLC	70752-102
Albuterol Sulfate	Albuterol sulfate 2 mg/5mL	SyrupOral	Bryant Ranch Prepack	71335-2907
Albuterol Sulfate	Albuterol sulfate 2 mg/5mL	SyrupOral	Bryant Ranch Prepack	72162-2064