formoterol fumarate
Generic: formoterol fumarate dihydrate
Labeler: devatis, inc.Drug Facts
Product Profile
Brand Name
formoterol fumarate
Generic Name
formoterol fumarate dihydrate
Labeler
devatis, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
formoterol fumarate 20 ug/2mL
Manufacturer
Identifiers & Regulatory
Product NDC
73043-051
Product ID
73043-051_7f289241-a13a-4a5f-b579-7b15dbab3d44
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218308
Listing Expiration
2026-12-31
Marketing Start
2025-06-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73043051
Hyphenated Format
73043-051
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
formoterol fumarate (source: ndc)
Generic Name
formoterol fumarate dihydrate (source: ndc)
Application Number
ANDA218308 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 ug/2mL
Packaging
- 30 POUCH in 1 CARTON (73043-051-93) / 1 VIAL in 1 POUCH / 2 mL in 1 VIAL
- 60 POUCH in 1 CARTON (73043-051-96) / 1 VIAL in 1 POUCH / 2 mL in 1 VIAL
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "7f289241-a13a-4a5f-b579-7b15dbab3d44", "openfda": {"unii": ["W34SHF8J2K"], "rxcui": ["1246319"], "spl_set_id": ["fd0dac5d-e58c-46ee-9d28-1a1ef7a6be5e"], "manufacturer_name": ["Devatis, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (73043-051-93) / 1 VIAL in 1 POUCH / 2 mL in 1 VIAL", "package_ndc": "73043-051-93", "marketing_start_date": "20250630"}, {"sample": false, "description": "60 POUCH in 1 CARTON (73043-051-96) / 1 VIAL in 1 POUCH / 2 mL in 1 VIAL", "package_ndc": "73043-051-96", "marketing_start_date": "20250630"}], "brand_name": "Formoterol fumarate", "product_id": "73043-051_7f289241-a13a-4a5f-b579-7b15dbab3d44", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "73043-051", "generic_name": "Formoterol fumarate dihydrate", "labeler_name": "Devatis, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Formoterol fumarate", "active_ingredients": [{"name": "FORMOTEROL FUMARATE", "strength": "20 ug/2mL"}], "application_number": "ANDA218308", "marketing_category": "ANDA", "marketing_start_date": "20250630", "listing_expiration_date": "20261231"}