NDC codes

FDA NDC Directory
Product NDC (as listed)67296-2338Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67296-2338Add 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
67296-2338-967296233809672962338096 POUCH in 1 CARTON (67296-2338-9) / 5 VIAL in 1 POUCH / 3 mL in 1 VIALMarketed from Jun 11, 2021

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 — .83 mg/mL
Dosage form
Solution
Route
Respiratory (Inhalation)
Labeler
Redpharm DrugNDC labeler code 67296
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207857
Marketing start
Listing expires
Other FDA classes
Adrenergic beta2-Agonists (Mechanism)
Identifiers
Product ID 67296-2338_5d6296ac-3e02-6bba-e063-6394a90af45bSPL ID 5d6296ac-3e02-6bba-e063-6394a90af45b
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

N467296233809 followed by a unit qualifier and the quantity

Package 67296-2338-09. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 67296-2338

What is NDC 67296-2338?
67296-2338 is the product NDC for Albuterol Sulfate, Albuterol sulfate .83 mg/mL solution, listed with the FDA by Redpharm Drug. 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?
Redpharm Drug, NDC labeler code 67296. 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 207857

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

FDA NDC Directory listings under ANDA 207857
ProductStrengthForm · routeLabelerProduct NDC
Albuterol SulfateAlbuterol sulfate .83 mg/mLSolutionRespiratory (Inhalation)Sun Pharmaceutical Industries, Inc.47335-703
Albuterol SulfateAlbuterol sulfate .83 mg/mLSolutionRespiratory (Inhalation)Preferred Pharmaceuticals Inc.68788-8492
Albuterol SulfateAlbuterol sulfate .83 mg/mLSolutionRespiratory (Inhalation)REMEDYREPACK INC.70518-3560
Albuterol SulfateAlbuterol sulfate .83 mg/mLSolutionRespiratory (Inhalation)Proficient Rx LP71205-641

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