albuterol sulfate
Generic: albuterol sulfate
Labeler: armstrong pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
albuterol sulfate
Generic Name
albuterol sulfate
Labeler
armstrong pharmaceuticals, inc.
Dosage Form
INHALANT
Routes
Active Ingredients
albuterol sulfate 90 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
17270-0740
Product ID
17270-0740_da039f76-a4c6-4463-a773-c433021a53e6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212447
Listing Expiration
2026-12-31
Marketing Start
2024-08-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
172700740
Hyphenated Format
17270-0740
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
albuterol sulfate (source: ndc)
Generic Name
albuterol sulfate (source: ndc)
Application Number
ANDA212447 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 90 ug/1
Packaging
- 1 INHALER in 1 CARTON (17270-0740-0) / 200 INHALANT 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": "da039f76-a4c6-4463-a773-c433021a53e6", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["17858afa-dcdf-4612-b475-3b6baadfb639"], "manufacturer_name": ["Armstrong Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (17270-0740-0) / 200 INHALANT in 1 INHALER", "package_ndc": "17270-0740-0", "marketing_start_date": "20240806"}], "brand_name": "Albuterol Sulfate", "product_id": "17270-0740_da039f76-a4c6-4463-a773-c433021a53e6", "dosage_form": "INHALANT", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "17270-0740", "generic_name": "Albuterol Sulfate", "labeler_name": "Armstrong Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "ANDA212447", "marketing_category": "ANDA", "marketing_start_date": "20240806", "listing_expiration_date": "20261231"}