albuterol sulfate
Generic: albuterol sulfate
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
albuterol sulfate
Generic Name
albuterol sulfate
Labeler
proficient rx lp
Dosage Form
AEROSOL, METERED
Routes
Active Ingredients
albuterol sulfate 90 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-732
Product ID
71205-732_4ed5342d-7933-406f-93f9-34f45b521ec6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209954
Listing Expiration
2026-12-31
Marketing Start
2020-08-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205732
Hyphenated Format
71205-732
Supplemental Identifiers
RxCUI
UPC
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
ANDA209954 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 90 ug/1
Packaging
- 1 CANISTER in 1 CARTON (71205-732-85) / 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": "4ed5342d-7933-406f-93f9-34f45b521ec6", "openfda": {"upc": ["0371205732851"], "unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["4100bce5-096c-42e4-9e4e-d11a0ab597d5"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 CANISTER in 1 CARTON (71205-732-85) / 200 AEROSOL, METERED in 1 CANISTER", "package_ndc": "71205-732-85", "marketing_start_date": "20221221"}], "brand_name": "Albuterol sulfate", "product_id": "71205-732_4ed5342d-7933-406f-93f9-34f45b521ec6", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "71205-732", "generic_name": "Albuterol sulfate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "ANDA209954", "marketing_category": "ANDA", "marketing_start_date": "20200825", "listing_expiration_date": "20261231"}