Albuterol sulfate solution

Ingredients and appearance - Product information

Albuterol sulfate solution- Albuterol sulfate

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 50436-2472
Route of Administration Intrabronchial

Active Ingredient/Active Moiety

Ingredient Name Strength
Albuterol sulfate ( UNII: 021SEF3731)( Albuterol - UNII: QF8SVZ843E ) 2.5 mgin 3 mL

Inactive Ingredients

Ingredient Name Code
Sodium chloride ( UNII: 451W47IQ8X)
Sulfuric acid ( UNII: O40UQP6WCF)

Product Characteristics

Packaging

# Item Code Package Description Marketing Start Date
1 NDC: 50436-2472-1 25mL in 1 CARTON 2015/04/28

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA077839 USA 2015/04/28

Labeler - Unit Dose Services( 831995316)

Establishment

Name ID/FEI Business Operations
Unit Dose Services 831995316 REPACK( 50436-2472), RELABEL( 50436-2472)

Albuterol sulfate solution

The finding of no arrhythmias and no palpitations after albuterol administration in this clinical study should not be interpreted as indicating that these adverse effects cannot occur after the administration of inhaled albuterol.
In most cases of bronchospasm, this term was generally used to describe exacerbations in the underlying pulmonary disease.