albuterol

Generic: albuterol

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

Drug Facts

Product Profile

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

albuterol sulfate 4 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-2611
Product ID 63629-2611_3352d236-01ed-a102-e063-6294a90a2a8d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207046
Listing Expiration 2026-12-31
Marketing Start 2018-06-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 636292611
Hyphenated Format 63629-2611

Supplemental Identifiers

RxCUI
197318
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 (source: ndc)
Generic Name albuterol (source: ndc)
Application Number ANDA207046 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (63629-2611-1)
  • 30 TABLET in 1 BOTTLE (63629-2611-2)
  • 60 TABLET in 1 BOTTLE (63629-2611-3)
source: ndc

Packages (3)

63629-2611-1 20 TABLET in 1 BOTTLE (63629-2611-1) 63629-2611-2 30 TABLET in 1 BOTTLE (63629-2611-2) 63629-2611-3 60 TABLET in 1 BOTTLE (63629-2611-3)

Ingredients (1)

albuterol sulfate (4 mg/1)

Linked Drug Pages (1)

Albuterol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3352d236-01ed-a102-e063-6294a90a2a8d", "openfda": {"unii": ["021SEF3731"], "rxcui": ["197318"], "spl_set_id": ["601a18ed-d66e-498f-a804-f1a3330827d4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (63629-2611-1)", "package_ndc": "63629-2611-1", "marketing_start_date": "20250408"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-2611-2)", "package_ndc": "63629-2611-2", "marketing_start_date": "20250408"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-2611-3)", "package_ndc": "63629-2611-3", "marketing_start_date": "20250408"}], "brand_name": "Albuterol", "product_id": "63629-2611_3352d236-01ed-a102-e063-6294a90a2a8d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "63629-2611", "generic_name": "albuterol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "4 mg/1"}], "application_number": "ANDA207046", "marketing_category": "ANDA", "marketing_start_date": "20180629", "listing_expiration_date": "20261231"}