Package 75834-273-01

Brand: albuterol

Generic: albuterol sulfate
NDC Package

Package Facts

Identity

Package NDC 75834-273-01
Digits Only 7583427301
Product NDC 75834-273
Product ID 75834-273_5b89a3bb-e3bb-421d-89f7-f180e01a1b4d
Description

100 TABLET in 1 BOTTLE, PLASTIC (75834-273-01)

Marketing

Marketing Status
Marketed Since 2021-01-21
Brand albuterol
Generic albuterol sulfate
Sample Package No

Linked Drug Pages (1)

Albuterol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5b89a3bb-e3bb-421d-89f7-f180e01a1b4d", "openfda": {"upc": ["0375834274010", "0375834273013"], "unii": ["021SEF3731"], "rxcui": ["197316", "197318"], "spl_set_id": ["b735e92d-eb1a-6fc1-e053-2995a90afce2"], "manufacturer_name": ["Nivagen Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (75834-273-01)", "package_ndc": "75834-273-01", "marketing_start_date": "20210121"}], "brand_name": "Albuterol", "product_id": "75834-273_5b89a3bb-e3bb-421d-89f7-f180e01a1b4d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "75834-273", "generic_name": "albuterol sulfate", "labeler_name": "Nivagen Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2 mg/1"}], "application_number": "ANDA210948", "marketing_category": "ANDA", "marketing_start_date": "20210121", "listing_expiration_date": "20261231"}