albuterol sulfate
Generic: albuterol sulfate
Labeler: sandoz incDrug Facts
Product Profile
Brand Name
albuterol sulfate
Generic Name
albuterol sulfate
Labeler
sandoz inc
Dosage Form
AEROSOL, METERED
Routes
Active Ingredients
albuterol sulfate 108 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
0781-7296
Product ID
0781-7296_44ec30c6-e178-d2ed-e063-6394a90a25a5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA020503
Listing Expiration
2026-12-31
Marketing Start
2021-03-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07817296
Hyphenated Format
0781-7296
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
NDA020503 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 108 ug/1
Packaging
- 1 CANISTER in 1 CARTON (0781-7296-85) / 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": "44ec30c6-e178-d2ed-e063-6394a90a25a5", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123111"], "spl_set_id": ["f8a2c4b7-a162-48ab-90b0-350e4da25c66"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 CANISTER in 1 CARTON (0781-7296-85) / 200 AEROSOL, METERED in 1 CANISTER", "package_ndc": "0781-7296-85", "marketing_start_date": "20210315"}], "brand_name": "Albuterol Sulfate", "product_id": "0781-7296_44ec30c6-e178-d2ed-e063-6394a90a25a5", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "0781-7296", "generic_name": "Albuterol Sulfate", "labeler_name": "Sandoz 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": "20210315", "listing_expiration_date": "20261231"}