albuterol sulfate
Generic: albuterol sulfate
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
albuterol sulfate
Generic Name
albuterol sulfate
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
AEROSOL, METERED
Routes
Active Ingredients
albuterol sulfate 90 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1513
Product ID
51662-1513_ef7c1f9d-3076-5fc6-e053-2a95a90aafec
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203760
Listing Expiration
2026-12-31
Marketing Start
2020-08-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621513
Hyphenated Format
51662-1513
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
ANDA203760 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 90 ug/1
Packaging
- 1 INHALER in 1 CARTON (51662-1513-1) / 200 AEROSOL, METERED 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": "ef7c1f9d-3076-5fc6-e053-2a95a90aafec", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123072"], "spl_set_id": ["ad299502-8779-d280-e053-2995a90a7371"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (51662-1513-1) / 200 AEROSOL, METERED in 1 INHALER", "package_ndc": "51662-1513-1", "marketing_start_date": "20200818"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "51662-1513_ef7c1f9d-3076-5fc6-e053-2a95a90aafec", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "51662-1513", "generic_name": "ALBUTEROL SULFATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALBUTEROL SULFATE", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "90 ug/1"}], "application_number": "ANDA203760", "marketing_category": "ANDA", "marketing_start_date": "20200818", "listing_expiration_date": "20261231"}