albuterol sulfate

Generic: albuterol sulfate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name albuterol sulfate
Generic Name albuterol sulfate
Labeler bryant ranch prepack
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

albuterol sulfate 2 mg/5mL

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2064
Product ID 72162-2064_04fd53e4-2877-4738-b62b-527b3770ba4c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212197
Listing Expiration 2026-12-31
Marketing Start 2019-09-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622064
Hyphenated Format 72162-2064

Supplemental Identifiers

RxCUI
755497
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 ANDA212197 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (72162-2064-2)
source: ndc

Packages (1)

Ingredients (1)

albuterol sulfate (2 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "04fd53e4-2877-4738-b62b-527b3770ba4c", "openfda": {"unii": ["021SEF3731"], "rxcui": ["755497"], "spl_set_id": ["45e07bdd-78f9-4055-9de3-646e67de7eaf"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (72162-2064-2)", "package_ndc": "72162-2064-2", "marketing_start_date": "20230815"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "72162-2064_04fd53e4-2877-4738-b62b-527b3770ba4c", "dosage_form": "SYRUP", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "72162-2064", "generic_name": "ALBUTEROL SULFATE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALBUTEROL SULFATE", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2 mg/5mL"}], "application_number": "ANDA212197", "marketing_category": "ANDA", "marketing_start_date": "20190906", "listing_expiration_date": "20261231"}