NDC codes

FDA NDC Directory
Product NDC (as listed)62135-827Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62135-0827Add 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
62135-827-846213508278430 POUCH in 1 CARTON (62135-827-84) / 1 VIAL in 1 POUCH / 3 mL in 1 VIALMarketed from Jan 19, 2024

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 — 1.25 mg/3mL
Dosage form
Solution
Route
Respiratory (Inhalation)
Labeler
Chartwell RX, LLCNDC labeler code 62135
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076355
Marketing start
Listing expires
Other FDA classes
Adrenergic beta2-Agonists (Mechanism)
Identifiers
Product ID 62135-827_11e59625-431b-e530-e063-6294a90a0596SPL ID 11e59625-431b-e530-e063-6294a90a0596SPL set ID 4e48ccbe-3ec0-4bf2-be28-83eb9baa63d6RxCUI 351136, 351137UNII 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 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

N462135082784 followed by a unit qualifier and the quantity

Package 62135-0827-84. 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 AND USAGE Albuterol sulfate inhalation solution is indicated for the relief of bronchospasm in patients 2 to 12 years of age with asthma (reversible obstructive airway disease).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62135-827

What is NDC 62135-827?
62135-827 is the product NDC for Albuterol Sulfate, Albuterol sulfate 1.25 mg/3mL solution, listed with the FDA by Chartwell RX, LLC. 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?
Chartwell RX, LLC, NDC labeler code 62135. 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?
90 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Albuterol SulfateAlbuterol sulfate 108 ug/1Aerosol, MeteredRespiratory (Inhalation)REMEDYREPACK INC.70518-452870518-4528-00
Albuterol SulfateAlbuterol sulfate 90 ug/1InhalantRespiratory (Inhalation)Preferred Pharmaceuticals, Inc.68788-404168788-4041-02
Albuterol SulfateAlbuterol sulfate 90 ug/1InhalantRespiratory (Inhalation)REMEDYREPACK INC.70518-449670518-4496-00
Albuterol SulfateAlbuterol sulfate .83 mg/mLSolutionRespiratory (Inhalation)REMEDYREPACK INC.70518-449070518-4490-00
Albuterol sulfateAlbuterol sulfate 90 ug/1Aerosol, MeteredRespiratory (Inhalation)Preferred Pharmaceuticals, Inc.68788-887868788-8878-02
Albuterol SulfateAlbuterol sulfate 90 ug/1InhalantRespiratory (Inhalation)Preferred Pharmaceuticals Inc.68788-887468788-8874-02
Albuterol SulfateAlbuterol sulfate 2.5 mg/.5mLSolutionRespiratory (Inhalation)Rising Pharma Holdings, Inc.64980-64264980-0642-03
Albuterol SulfateAlbuterol sulfate .63 mg/3mLSolutionRespiratory (Inhalation)Rising Pharma Holdings, Inc64980-64364980-0643-03
Albuterol SulfateAlbuterol sulfate 1.25 mg/3mLSolutionRespiratory (Inhalation)Rising Pharma Holdings, Inc64980-64464980-0644-02
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Rising Pharma Holdings, Inc.64980-64164980-0641-0264980-0641-0364980-0641-06

All 91 Albuterol Sulfate NDCs

Other NDCs under ANDA 076355

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

FDA NDC Directory listings under ANDA 076355
ProductStrengthForm · routeLabelerProduct NDC
Albuterol SulfateAlbuterol sulfate .63 mg/3mLSolutionRespiratory (Inhalation)Nephron Pharmaceuticals Corporation0487-0301
Albuterol SulfateAlbuterol sulfate 1.25 mg/3mLSolutionRespiratory (Inhalation)Nephron Pharmaceuticals Corporation0487-9904
Albuterol SulfateAlbuterol sulfate .63 mg/3mLSolutionRespiratory (Inhalation)Chartwell RX, LLC62135-826
Albuterol SulfateAlbuterol sulfate .63 mg/3mLSolutionRespiratory (Inhalation)Rising Pharma Holdings, Inc64980-643
Albuterol SulfateAlbuterol sulfate 1.25 mg/3mLSolutionRespiratory (Inhalation)Rising Pharma Holdings, Inc64980-644

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