arformoterol tartrate

Generic: arformoterol tartrate

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name arformoterol tartrate
Generic Name arformoterol tartrate
Labeler northstar rxllc
Dosage Form SOLUTION
Routes
RESPIRATORY (INHALATION)
Active Ingredients

arformoterol tartrate 15 ug/2mL

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-208
Product ID 72603-208_c3d670fd-671b-4c32-a9ca-448dc6a49c66
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216128
Listing Expiration 2026-12-31
Marketing Start 2024-06-01

Pharmacologic Class

Classes
adrenergic beta2-agonists [moa] beta2-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603208
Hyphenated Format 72603-208

Supplemental Identifiers

RxCUI
668956
UNII
5P8VJ2I235

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name arformoterol tartrate (source: ndc)
Generic Name arformoterol tartrate (source: ndc)
Application Number ANDA216128 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • 15 ug/2mL
source: ndc
Packaging
  • 30 POUCH in 1 CARTON (72603-208-30) / 1 VIAL in 1 POUCH (72603-208-01) / 2 mL in 1 VIAL
  • 60 POUCH in 1 CARTON (72603-208-60) / 4 VIAL in 1 POUCH (72603-208-04) / 2 mL in 1 VIAL
source: ndc

Packages (2)

72603-208-30 30 POUCH in 1 CARTON (72603-208-30) / 1 VIAL in 1 POUCH (72603-208-01) / 2 mL in 1 VIAL 72603-208-60 60 POUCH in 1 CARTON (72603-208-60) / 4 VIAL in 1 POUCH (72603-208-04) / 2 mL in 1 VIAL

Ingredients (1)

arformoterol tartrate (15 ug/2mL)

Linked Drug Pages (1)

arformoterol tartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "c3d670fd-671b-4c32-a9ca-448dc6a49c66", "openfda": {"unii": ["5P8VJ2I235"], "rxcui": ["668956"], "spl_set_id": ["6a498c49-042f-481f-bc5c-a2fc00dc5668"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (72603-208-30)  / 1 VIAL in 1 POUCH (72603-208-01)  / 2 mL in 1 VIAL", "package_ndc": "72603-208-30", "marketing_start_date": "20240601"}, {"sample": false, "description": "60 POUCH in 1 CARTON (72603-208-60)  / 4 VIAL in 1 POUCH (72603-208-04)  / 2 mL in 1 VIAL", "package_ndc": "72603-208-60", "marketing_start_date": "20240601"}], "brand_name": "arformoterol tartrate", "product_id": "72603-208_c3d670fd-671b-4c32-a9ca-448dc6a49c66", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "72603-208", "generic_name": "arformoterol tartrate", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "arformoterol tartrate", "active_ingredients": [{"name": "ARFORMOTEROL TARTRATE", "strength": "15 ug/2mL"}], "application_number": "ANDA216128", "marketing_category": "ANDA", "marketing_start_date": "20240601", "listing_expiration_date": "20261231"}