Product Details for NDA 019243
PROVENTIL (ALBUTEROL SULFATE)
EQ 0.083% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 0.5% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
EQ 0.083% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: ALBUTEROL SULFATE
Proprietary Name: PROVENTIL
Dosage Form; Route of Administration: SOLUTION; INHALATION
Strength: EQ 0.083% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019243
Product Number: 002
Approval Date: Jan 14, 1987
Applicant Holder Full Name: SCHERING CORP SUB SCHERING PLOUGH CORP
Marketing Status: Discontinued
Patent and Exclusivity Information
PROVENTIL (ALBUTEROL SULFATE)
Proprietary Name: PROVENTIL
Dosage Form; Route of Administration: SOLUTION; INHALATION
Strength: EQ 0.083% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019243
Product Number: 002
Approval Date: Jan 14, 1987
Applicant Holder Full Name: SCHERING CORP SUB SCHERING PLOUGH CORP
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 0.5% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: ALBUTEROL SULFATE
Proprietary Name: PROVENTIL
Dosage Form; Route of Administration: SOLUTION; INHALATION
Strength: EQ 0.5% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019243
Product Number: 001
Approval Date: Jan 14, 1987
Applicant Holder Full Name: SCHERING CORP SUB SCHERING PLOUGH CORP
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: PROVENTIL
Dosage Form; Route of Administration: SOLUTION; INHALATION
Strength: EQ 0.5% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019243
Product Number: 001
Approval Date: Jan 14, 1987
Applicant Holder Full Name: SCHERING CORP SUB SCHERING PLOUGH CORP
Marketing Status: Discontinued
Patent and Exclusivity Information