NDC codes

FDA NDC Directory
Product NDC (as listed)72603-208Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72603-0208Add 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
72603-208-30726030208307260302083030 POUCH in 1 CARTON (72603-208-30) / 1 VIAL in 1 POUCH (72603-208-01) / 2 mL in 1 VIALMarketed from Jun 1, 2024
72603-208-60726030208607260302086060 POUCH in 1 CARTON (72603-208-60) / 4 VIAL in 1 POUCH (72603-208-04) / 2 mL in 1 VIALMarketed from Jun 1, 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)
arformoterol tartrate
Generic name (nonproprietary)
arformoterol tartrate
Active ingredients
Arformoterol tartrate — 15 ug/2mL
Dosage form
Solution
Route
Respiratory (Inhalation)
Labeler
NorthStar RxLLCNDC labeler code 72603
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216128
Marketing start
Listing expires
Other FDA classes
Adrenergic beta2-Agonists (Mechanism)
Identifiers
Product ID 72603-208_c3d670fd-671b-4c32-a9ca-448dc6a49c66SPL ID c3d670fd-671b-4c32-a9ca-448dc6a49c66SPL set ID 6a498c49-042f-481f-bc5c-a2fc00dc5668RxCUI 668956UNII 5P8VJ2I235
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

N472603020830 followed by a unit qualifier and the quantity

Package 72603-0208-30. 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)

Arformoterol tartrate inhalation solution is a long-acting beta 2 -adrenergic agonist (beta 2 -agonist) indicated for: Long-term, twice daily (morning and evening) administration in the maintenance treatment of bronchoconstriction in patients with chronic obstructive pulmonary disease (COPD), including chronic bronchitis and emphysema. ( 1.1 ). Important limitations of use: Arformoterol tartrate inhalation solution is not indicated to treat acute deteriorations of chronic obstructive pulmonary disease. (1.2, 5.2) Arformoterol tartrate inhalation solution is not indicated to treat asthma. (1.2) 1.1 Maintenance Treatment of COPD Arformoterol tartrate inhalation solution is indicated for the lo…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72603-208

What is NDC 72603-208?
72603-208 is the product NDC for arformoterol tartrate, Arformoterol tartrate 15 ug/2mL solution, listed with the FDA by NorthStar RxLLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
arformoterol tartrate.
What is the active ingredient?
Arformoterol tartrate.
Who is the labeler?
NorthStar RxLLC, NDC labeler code 72603. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for arformoterol tartrate?
10 other product NDCs are listed under this name. See all arformoterol tartrate 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 arformoterol tartrate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Arformoterol TartrateArformoterol tartrate 15 ug/2mLSolutionRespiratory (Inhalation)Micro Labs Limited42571-46442571-0464-73
Arformoterol tartrateArformoterol tartrate 15 ug/2mLSolutionRespiratory (Inhalation)Fosun Pharma USA Inc.72266-25972266-0259-3072266-0259-60
Arformoterol TartrateArformoterol tartrate 15 ug/2mLSolutionRespiratory (Inhalation)Ingenus Pharmaceuticals, LLC50742-39550742-0395-3050742-0395-60
arformoterol tartrateArformoterol tartrate 15 ug/2mLSolutionRespiratory (Inhalation)Dr. Reddy's Laboratories, Inc.43598-77743598-0777-3043598-0777-60
Arformoterol TartrateArformoterol tartrate 15 ug/2mLSolutionRespiratory (Inhalation)American Health Packaging60687-77060687-0770-8360687-0770-84
arformoterol tartrateArformoterol tartrate 15 ug/2mLSolutionRespiratory (Inhalation)Lifestar Pharma LLC70756-61270756-0612-6070756-0612-70
Arformoterol tartrateArformoterol tartrate 15 ug/2mLSolutionRespiratory (Inhalation)Lupin Pharmaceuticals, Inc.70748-17570748-0175-3070748-0175-60
Arformoterol TartrateArformoterol tartrate 15 ug/2mLSolutionRespiratory (Inhalation)Sun Pharmaceutical Industries, Inc.62756-27762756-0277-0262756-0277-03
Arformoterol tartrateArformoterol tartrate 15 ug/2mLSolutionRespiratory (Inhalation)Alembic Pharmaceuticals Inc.62332-63362332-0633-3062332-0633-60
arformoterol tartrateArformoterol tartrate 15 ug/2mLSolutionRespiratory (Inhalation)Cipla USA Inc.69097-16869097-0168-5369097-0168-6469097-0168-87

Other NDCs under ANDA 216128

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

FDA NDC Directory listings under ANDA 216128
ProductStrengthForm · routeLabelerProduct NDC
arformoterol tartrateArformoterol tartrate 15 ug/2mLSolutionRespiratory (Inhalation)Lifestar Pharma LLC70756-612

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