albuterol sulfate

Generic: albuterol sulfate

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name albuterol sulfate
Generic Name albuterol sulfate
Labeler hf acquisition co llc, dba healthfirst
Dosage Form SOLUTION
Routes
RESPIRATORY (INHALATION)
Active Ingredients

albuterol sulfate 2.5 mg/3mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1499
Product ID 51662-1499_2b387337-c48e-7eb1-e063-6294a90a9cba
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074880
Listing Expiration 2026-12-31
Marketing Start 2020-01-29

Pharmacologic Class

Classes
adrenergic beta2-agonists [moa] beta2-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621499
Hyphenated Format 51662-1499

Supplemental Identifiers

RxCUI
630208
UPC
0304879501003
UNII
021SEF3731

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 ANDA074880 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/3mL
source: ndc
Packaging
  • 5 VIAL, SINGLE-DOSE in 1 POUCH (51662-1499-1) / 3 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

51662-1499-1 5 VIAL, SINGLE-DOSE in 1 POUCH (51662-1499-1) / 3 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

albuterol sulfate (2.5 mg/3mL)

Linked Drug Pages (1)

ALBUTEROL SULFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "2b387337-c48e-7eb1-e063-6294a90a9cba", "openfda": {"upc": ["0304879501003"], "unii": ["021SEF3731"], "rxcui": ["630208"], "spl_set_id": ["9d4ef83f-8ca0-811e-e053-2995a90a6d0d"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL, SINGLE-DOSE in 1 POUCH (51662-1499-1)  / 3 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "51662-1499-1", "marketing_start_date": "20200129"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "51662-1499_2b387337-c48e-7eb1-e063-6294a90a9cba", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "51662-1499", "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": "2.5 mg/3mL"}], "application_number": "ANDA074880", "marketing_category": "ANDA", "marketing_start_date": "20200129", "listing_expiration_date": "20261231"}