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
AEROSOL, METERED
Routes
Active Ingredients
albuterol sulfate 108 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-7996
Product ID
68788-7996_b4d7b542-5aaa-4a4e-a73a-a2b193715cc8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA020503
Listing Expiration
2027-12-31
Marketing Start
2021-08-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887996
Hyphenated Format
68788-7996
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
NDA020503 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 108 ug/1
Packaging
- 1 CANISTER in 1 CARTON (68788-7996-2) / 200 AEROSOL, METERED in 1 CANISTER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "b4d7b542-5aaa-4a4e-a73a-a2b193715cc8", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123111"], "spl_set_id": ["d6acb5a7-555a-463a-ae65-2911d6789b42"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 CANISTER in 1 CARTON (68788-7996-2) / 200 AEROSOL, METERED in 1 CANISTER", "package_ndc": "68788-7996-2", "marketing_start_date": "20210810"}], "brand_name": "Albuterol Sulfate", "product_id": "68788-7996_b4d7b542-5aaa-4a4e-a73a-a2b193715cc8", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "68788-7996", "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": "108 ug/1"}], "application_number": "NDA020503", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20210810", "listing_expiration_date": "20271231"}