NDC codes

FDA NDC Directory
Product NDC (as listed)51662-1499Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51662-1499Add 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 NDC11-digit (billing)PackageCopy
51662-1499-1516621499015 VIAL, SINGLE-DOSE in 1 POUCH (51662-1499-1) / 3 mL in 1 VIAL, SINGLE-DOSEMarketed from Jan 29, 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 — 2.5 mg/3mL
Dosage form
Solution
Route
Respiratory (Inhalation)
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074880
Marketing start
Listing expires
Other FDA classes
Adrenergic beta2-Agonists (Mechanism)
Identifiers
Product ID 51662-1499_2b387337-c48e-7eb1-e063-6294a90a9cbaSPL ID 2b387337-c48e-7eb1-e063-6294a90a9cbaSPL set ID 9d4ef83f-8ca0-811e-e053-2995a90a6d0dRxCUI 630208UNII 021SEF3731UPC 0304879501003
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

N451662149901 followed by a unit qualifier and the quantity

Package 51662-1499-01. 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 .

Indications (excerpt from the label)

INDICATIONS & USAGE Albuterol sulfate inhalation solution is indicated for the relief of bronchospasm in patients 2 years of age and older with reversible obstructive airway disease and acute attacks of bronchospasm.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 074880

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

FDA NDC Directory listings under ANDA 074880
ProductStrengthForm · routeLabelerProduct NDC
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Proficient Rx LP63187-204
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Rising Pharma Holdings, Inc.64980-641
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)NuCare Pharmaceuticals,Inc.68071-4543
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Chartwell RX, LLC62135-828
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)NuCare Pharmaceuticals,Inc.68071-4754
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Nephron Pharmaceuticals Corporation0487-9501
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)ASCLEMED USA INC.87063-031
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Sportpharm LLC85766-127
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Asclemed USA, Inc.76420-087
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)A-S Medication Solutions50090-6560
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Asclemed USA, Inc.76420-087

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