albuterol sulfate
Generic: albuterol sulfate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
albuterol sulfate
Generic Name
albuterol sulfate
Labeler
a-s medication solutions
Dosage Form
SOLUTION
Routes
Active Ingredients
albuterol sulfate 2.5 mg/3mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6560
Product ID
50090-6560_9e4a9dac-8e00-4b2d-b3a1-2c9826e32e66
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074880
Listing Expiration
2026-12-31
Marketing Start
1997-09-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906560
Hyphenated Format
50090-6560
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 (source: ndc)
Generic Name
albuterol sulfate (source: ndc)
Application Number
ANDA074880 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2.5 mg/3mL
Packaging
- 25 POUCH in 1 CARTON (50090-6560-0) / 3 mL in 1 POUCH
- 75 POUCH in 1 CARTON (50090-6560-1) / 3 mL in 1 POUCH
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "9e4a9dac-8e00-4b2d-b3a1-2c9826e32e66", "openfda": {"unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["8f52f15f-3fb7-4b00-a19f-8721c5ac55db"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "25 POUCH in 1 CARTON (50090-6560-0) / 3 mL in 1 POUCH", "package_ndc": "50090-6560-0", "marketing_start_date": "20230717"}, {"sample": false, "description": "75 POUCH in 1 CARTON (50090-6560-1) / 3 mL in 1 POUCH", "package_ndc": "50090-6560-1", "marketing_start_date": "20230724"}], "brand_name": "Albuterol Sulfate", "product_id": "50090-6560_9e4a9dac-8e00-4b2d-b3a1-2c9826e32e66", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "50090-6560", "generic_name": "Albuterol Sulfate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2.5 mg/3mL"}], "application_number": "ANDA074880", "marketing_category": "ANDA", "marketing_start_date": "19970917", "listing_expiration_date": "20261231"}