Product Details for NDA 016472
MANNITOL 10% (MANNITOL)
10GM/100ML
Marketing Status: Discontinued
15GM/100ML
Marketing Status: Discontinued
20GM/100ML
Marketing Status: Discontinued
10GM/100ML
Marketing Status: Discontinued
Active Ingredient: MANNITOL
Proprietary Name: MANNITOL 10%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10GM/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N016472
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MILES LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
MANNITOL 15% (MANNITOL)
Proprietary Name: MANNITOL 10%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10GM/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N016472
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MILES LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
15GM/100ML
Marketing Status: Discontinued
Active Ingredient: MANNITOL
Proprietary Name: MANNITOL 15%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 15GM/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N016472
Product Number: 005
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MILES LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
MANNITOL 20% (MANNITOL)
Proprietary Name: MANNITOL 15%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 15GM/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N016472
Product Number: 005
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MILES LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
20GM/100ML
Marketing Status: Discontinued
Active Ingredient: MANNITOL
Proprietary Name: MANNITOL 20%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20GM/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N016472
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MILES LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: MANNITOL 20%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20GM/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N016472
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MILES LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information