albuterol sulfate hfa
Generic: albuterol sulfate
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
albuterol sulfate hfa
Generic Name
albuterol sulfate
Labeler
asclemed usa, inc.
Dosage Form
AEROSOL, METERED
Routes
Active Ingredients
albuterol sulfate 90 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
76420-088
Product ID
76420-088_0cdb4881-c3c2-9edf-e063-6394a90a5cac
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA021457
Listing Expiration
2026-12-31
Marketing Start
2019-01-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420088
Hyphenated Format
76420-088
Supplemental Identifiers
RxCUI
UNII
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
albuterol sulfate hfa (source: ndc)
Generic Name
albuterol sulfate (source: ndc)
Application Number
NDA021457 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 90 ug/1
Packaging
- 1 INHALER in 1 CARTON (76420-088-01) / 200 AEROSOL, METERED in 1 INHALER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "0cdb4881-c3c2-9edf-e063-6394a90a5cac", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["a69489f7-4ffb-4cd1-b2d2-002f48e84f51"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (76420-088-01) / 200 AEROSOL, METERED in 1 INHALER", "package_ndc": "76420-088-01", "marketing_start_date": "20201013"}], "brand_name": "Albuterol Sulfate HFA", "product_id": "76420-088_0cdb4881-c3c2-9edf-e063-6394a90a5cac", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "76420-088", "generic_name": "Albuterol Sulfate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "brand_name_suffix": "HFA", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "NDA021457", "marketing_category": "NDA", "marketing_start_date": "20190116", "listing_expiration_date": "20261231"}