albuterol sulfate

Generic: albuterol sulfate

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

Drug Facts

Product Profile

Brand Name albuterol sulfate
Generic Name albuterol sulfate
Labeler armstrong pharmaceuticals, inc.
Dosage Form INHALANT
Routes
RESPIRATORY (INHALATION)
Active Ingredients

albuterol sulfate 90 ug/1

Manufacturer
Armstrong Pharmaceuticals, Inc.

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 172700740
Hyphenated Format 17270-0740

Supplemental Identifiers

RxCUI
2123072
UNII
021SEF3731

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 albuterol sulfate (source: ndc)
Generic Name albuterol sulfate (source: ndc)
Application Number ANDA212447 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • 90 ug/1
source: ndc
Packaging
  • 1 INHALER in 1 CARTON (17270-0740-0) / 200 INHALANT in 1 INHALER
source: ndc

Packages (1)

Ingredients (1)

albuterol sulfate (90 ug/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"}