albuterol

Generic: albuterol

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name albuterol
Generic Name albuterol
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

albuterol sulfate 4 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-899
Product ID 71205-899_f5ac6375-7f17-4d27-b13a-b44e73281838
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 71205899
Hyphenated Format 71205-899

Supplemental Identifiers

RxCUI
197316 197318
UPC
0371205898304 0371205899301
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
  • 100 TABLET in 1 BOTTLE (71205-899-00)
  • 1000 TABLET in 1 BOTTLE (71205-899-11)
  • 30 TABLET in 1 BOTTLE (71205-899-30)
  • 500 TABLET in 1 BOTTLE (71205-899-55)
  • 60 TABLET in 1 BOTTLE (71205-899-60)
  • 90 TABLET in 1 BOTTLE (71205-899-90)
source: ndc

Packages (6)

71205-899-00 100 TABLET in 1 BOTTLE (71205-899-00) 71205-899-11 1000 TABLET in 1 BOTTLE (71205-899-11) 71205-899-30 30 TABLET in 1 BOTTLE (71205-899-30) 71205-899-55 500 TABLET in 1 BOTTLE (71205-899-55) 71205-899-60 60 TABLET in 1 BOTTLE (71205-899-60) 71205-899-90 90 TABLET in 1 BOTTLE (71205-899-90)

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": "f5ac6375-7f17-4d27-b13a-b44e73281838", "openfda": {"upc": ["0371205898304", "0371205899301"], "unii": ["021SEF3731"], "rxcui": ["197316", "197318"], "spl_set_id": ["895dff1c-d21c-4470-b021-a5b68364c1ec"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71205-899-00)", "package_ndc": "71205-899-00", "marketing_start_date": "20210730"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71205-899-11)", "package_ndc": "71205-899-11", "marketing_start_date": "20210730"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-899-30)", "package_ndc": "71205-899-30", "marketing_start_date": "20210730"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71205-899-55)", "package_ndc": "71205-899-55", "marketing_start_date": "20210730"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-899-60)", "package_ndc": "71205-899-60", "marketing_start_date": "20210730"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-899-90)", "package_ndc": "71205-899-90", "marketing_start_date": "20210730"}], "brand_name": "Albuterol", "product_id": "71205-899_f5ac6375-7f17-4d27-b13a-b44e73281838", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "71205-899", "generic_name": "albuterol", "labeler_name": "Proficient Rx LP", "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"}