Levalbuterol (levalbuterol hydrochloride) NDC 50090-6377

Product information

Brand name (proprietary)

Levalbuterol

Generic name (nonproprietary)

levalbuterol hydrochloride

Active ingredients

Levalbuterol hydrochloride — .63 mg/3mL

Dosage form

Solution

Route

Respiratory (Inhalation)

Labeler

A-S Medication Solutions

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 203653

Marketing start

Apr 1, 2021

Listing expires

Dec 31, 2026

Other FDA classes

Adrenergic beta2-Agonists (Mechanism)

Identifiers

Product ID 50090-6377_9c6c8e7b-61bd-437b-ba6e-cb394ad19d16SPL ID 9c6c8e7b-61bd-437b-ba6e-cb394ad19d16SPL set ID 262c0b8b-8461-4bdf-b272-c829d33fd451RxCUI 311286UNII WDQ1526QJM

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

N450090637700 followed by a unit qualifier and the quantity Copy

Package 50090-6377-00. 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

Other NDCs under ANDA 203653

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