arformoterol tartrate inhalation

Generic: arformoterol tartrate inhalation

Labeler: devatis, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name arformoterol tartrate inhalation
Generic Name arformoterol tartrate inhalation
Labeler devatis, inc.
Dosage Form SOLUTION
Routes
RESPIRATORY (INHALATION)
Active Ingredients

arformoterol tartrate 15 ug/2mL

Manufacturer
Devatis, Inc.

Identifiers & Regulatory

Product NDC 73043-052
Product ID 73043-052_8f1bd281-a307-4e2c-8796-6b55495bd3e2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218429
Listing Expiration 2026-12-31
Marketing Start 2025-08-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73043052
Hyphenated Format 73043-052

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 inhalation (source: ndc)
Generic Name arformoterol tartrate inhalation (source: ndc)
Application Number ANDA218429 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • 15 ug/2mL
source: ndc
Packaging
  • 60 POUCH in 1 CARTON (73043-052-60) / 4 VIAL in 1 POUCH (73043-052-04) / 2 mL in 1 VIAL
  • 30 POUCH in 1 CARTON (73043-052-93) / 1 VIAL in 1 POUCH (73043-052-01) / 2 mL in 1 VIAL
source: ndc

Packages (2)

73043-052-60 60 POUCH in 1 CARTON (73043-052-60) / 4 VIAL in 1 POUCH (73043-052-04) / 2 mL in 1 VIAL 73043-052-93 30 POUCH in 1 CARTON (73043-052-93) / 1 VIAL in 1 POUCH (73043-052-01) / 2 mL in 1 VIAL

Ingredients (1)

arformoterol tartrate (15 ug/2mL)

Linked Drug Pages (1)

Arformoterol Tartrate Inhalation ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "8f1bd281-a307-4e2c-8796-6b55495bd3e2", "openfda": {"unii": ["5P8VJ2I235"], "rxcui": ["668956"], "spl_set_id": ["a4b5c1fd-6dee-4c0a-a7c6-b6baaba2bb99"], "manufacturer_name": ["Devatis, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 POUCH in 1 CARTON (73043-052-60)  / 4 VIAL in 1 POUCH (73043-052-04)  / 2 mL in 1 VIAL", "package_ndc": "73043-052-60", "marketing_start_date": "20250801"}, {"sample": false, "description": "30 POUCH in 1 CARTON (73043-052-93)  / 1 VIAL in 1 POUCH (73043-052-01)  / 2 mL in 1 VIAL", "package_ndc": "73043-052-93", "marketing_start_date": "20250801"}], "brand_name": "Arformoterol Tartrate Inhalation", "product_id": "73043-052_8f1bd281-a307-4e2c-8796-6b55495bd3e2", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "73043-052", "generic_name": "Arformoterol Tartrate Inhalation", "labeler_name": "Devatis, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Arformoterol Tartrate Inhalation", "active_ingredients": [{"name": "ARFORMOTEROL TARTRATE", "strength": "15 ug/2mL"}], "application_number": "ANDA218429", "marketing_category": "ANDA", "marketing_start_date": "20250801", "listing_expiration_date": "20261231"}