NDC codes

FDA NDC Directory
Product NDC (as listed)63187-204Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63187-0204Add 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
63187-204-2563187020425631870204251 POUCH in 1 CARTON (63187-204-25) / 25 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSEMarketed from Nov 1, 2018

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 — 2.5 mg/3mL
Dosage form
Solution
Route
Respiratory (Inhalation)
Labeler
Proficient Rx LPNDC labeler code 63187
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 63187-204_621471a7-e06e-4d18-be4b-aca66c225a39SPL ID 621471a7-e06e-4d18-be4b-aca66c225a39SPL set ID d3d2ab1e-8f91-4a4d-aa6b-5a57f59ad56bRxCUI 630208UNII 021SEF3731UPC 0363187204259
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

N463187020425 followed by a unit qualifier and the quantity

Package 63187-0204-25. 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 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)

About NDC 63187-204

What is NDC 63187-204?
63187-204 is the product NDC for Albuterol Sulfate, Albuterol sulfate 2.5 mg/3mL solution, listed with the FDA by Proficient Rx LP. 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?
Proficient Rx LP, NDC labeler code 63187. 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?
91 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 92 Albuterol Sulfate NDCs

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)Nephron Pharmaceuticals Corporation0487-9501
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)A-S Medication Solutions50090-6560
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)HF Acquisition Co LLC, DBA HealthFirst51662-1499
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Chartwell RX, LLC62135-828
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)NuCare Pharmaceuticals,Inc.68071-4754
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Asclemed USA, Inc.76420-087
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)Sportpharm LLC85766-127
Albuterol SulfateAlbuterol sulfate 2.5 mg/3mLSolutionRespiratory (Inhalation)ASCLEMED USA INC.87063-031

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