arformoterol tartrate

Generic: arformoterol tartrate

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name arformoterol tartrate
Generic Name arformoterol tartrate
Labeler teva pharmaceuticals usa, inc.
Dosage Form SOLUTION
Routes
RESPIRATORY (INHALATION)
Active Ingredients

arformoterol tartrate 15 ug/2mL

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-5955
Product ID 0093-5955_98de9422-52ec-42d8-b4c4-f3ad3b11460f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200293
Listing Expiration 2026-12-31
Marketing Start 2021-12-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00935955
Hyphenated Format 0093-5955

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 ANDA200293 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • 15 ug/2mL
source: ndc
Packaging
  • 12 POUCH in 1 CARTON (0093-5955-06) / 5 AMPULE in 1 POUCH (0093-5955-45) / 2 mL in 1 AMPULE (0093-5955-19)
  • 30 POUCH in 1 CARTON (0093-5955-56) / 1 AMPULE in 1 POUCH (0093-5955-11) / 2 mL in 1 AMPULE
source: ndc

Packages (2)

0093-5955-06 12 POUCH in 1 CARTON (0093-5955-06) / 5 AMPULE in 1 POUCH (0093-5955-45) / 2 mL in 1 AMPULE (0093-5955-19) 0093-5955-56 30 POUCH in 1 CARTON (0093-5955-56) / 1 AMPULE in 1 POUCH (0093-5955-11) / 2 mL in 1 AMPULE

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": "98de9422-52ec-42d8-b4c4-f3ad3b11460f", "openfda": {"unii": ["5P8VJ2I235"], "rxcui": ["668956"], "spl_set_id": ["07210cd5-679f-4834-8b77-724583e4c9c8"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CARTON (0093-5955-06)  / 5 AMPULE in 1 POUCH (0093-5955-45)  / 2 mL in 1 AMPULE (0093-5955-19)", "package_ndc": "0093-5955-06", "marketing_start_date": "20211206"}, {"sample": false, "description": "30 POUCH in 1 CARTON (0093-5955-56)  / 1 AMPULE in 1 POUCH (0093-5955-11)  / 2 mL in 1 AMPULE", "package_ndc": "0093-5955-56", "marketing_start_date": "20211206"}], "brand_name": "Arformoterol tartrate", "product_id": "0093-5955_98de9422-52ec-42d8-b4c4-f3ad3b11460f", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "0093-5955", "generic_name": "Arformoterol tartrate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Arformoterol tartrate", "active_ingredients": [{"name": "ARFORMOTEROL TARTRATE", "strength": "15 ug/2mL"}], "application_number": "ANDA200293", "marketing_category": "ANDA", "marketing_start_date": "20211206", "listing_expiration_date": "20261231"}