albuterol sulate hfa
Generic: albuterol sulfate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
albuterol sulate hfa
Generic Name
albuterol sulfate
Labeler
remedyrepack inc.
Dosage Form
AEROSOL, METERED
Routes
Active Ingredients
albuterol sulfate 90 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-2072
Product ID
70518-2072_499c75ab-2f45-5ba7-e063-6394a90aecfc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA020983
Listing Expiration
2027-12-31
Marketing Start
2019-05-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705182072
Hyphenated Format
70518-2072
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 sulate hfa (source: ndc)
Generic Name
albuterol sulfate (source: ndc)
Application Number
NDA020983 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 90 ug/1
Packaging
- 1 INHALER in 1 CARTON (70518-2072-0) / 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": "499c75ab-2f45-5ba7-e063-6394a90aecfc", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123076"], "spl_set_id": ["77d34a3c-ccc6-420a-ad31-a1af55f7de76"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (70518-2072-0) / 200 AEROSOL, METERED in 1 INHALER", "package_ndc": "70518-2072-0", "marketing_start_date": "20190513"}], "brand_name": "Albuterol Sulate HFA", "product_id": "70518-2072_499c75ab-2f45-5ba7-e063-6394a90aecfc", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70518-2072", "generic_name": "albuterol sulfate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulate", "brand_name_suffix": "HFA", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "NDA020983", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190513", "listing_expiration_date": "20271231"}