Albuterol Sulfate NDC 70752-102

NDC codes

FDA NDC Directory

Product NDC (as listed)70752-102Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70752-0102Add 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
70752-102-12	70752010212	473 mL in 1 BOTTLE (70752-102-12)Marketed from Sep 6, 2019

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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: QUAGEN PHARMACEUTICALS LLC
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 70752-102_f8b35fdc-741f-4ebd-91d5-a55a7ef8e261SPL ID f8b35fdc-741f-4ebd-91d5-a55a7ef8e261SPL set ID 99a490cc-e41d-436b-9cf3-8facb7ac714fRxCUI 755497UNII 021SEF3731UPC 0370752102124
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

N470752010212 followed by a unit qualifier and the quantity

Package 70752-0102-12. 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 Jul 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	Bryant Ranch Prepack	71335-2907
Albuterol Sulfate	Albuterol sulfate 2 mg/5mL	SyrupOral	Preferred Pharmaceuticals, Inc.	68788-7573
Albuterol Sulfate	Albuterol sulfate 2 mg/5mL	SyrupOral	Bryant Ranch Prepack	72162-2064