albuterol sulfate
Generic: albuterol sulfate
Labeler: preferred pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
albuterol sulfate
Generic Name
albuterol sulfate
Labeler
preferred pharmaceuticals, inc.
Dosage Form
INHALANT
Routes
Active Ingredients
albuterol sulfate 90 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-4041
Product ID
68788-4041_081b7bbb-6692-4512-b135-863b73bf30a5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212447
Listing Expiration
2026-12-31
Marketing Start
2025-10-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687884041
Hyphenated Format
68788-4041
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
ANDA212447 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 90 ug/1
Packaging
- 1 INHALER in 1 CARTON (68788-4041-2) / 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": "081b7bbb-6692-4512-b135-863b73bf30a5", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["081b7bbb-6692-4512-b135-863b73bf30a5"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (68788-4041-2) / 200 INHALANT in 1 INHALER", "package_ndc": "68788-4041-2", "marketing_start_date": "20251013"}], "brand_name": "Albuterol Sulfate", "product_id": "68788-4041_081b7bbb-6692-4512-b135-863b73bf30a5", "dosage_form": "INHALANT", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68788-4041", "generic_name": "Albuterol Sulfate", "labeler_name": "Preferred 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": "20251013", "listing_expiration_date": "20261231"}