Product Details for NDA 018685
GAVISCON (ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE)
80MG;20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
160MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
80MG;20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE
Proprietary Name: GAVISCON
Dosage Form; Route of Administration: TABLET, CHEWABLE; ORAL
Strength: 80MG;20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N018685
Product Number: 001
Approval Date: Dec 9, 1983
Applicant Holder Full Name: CHATTEM INC DBA SANOFI CONSUMER HEALTHCARE
Marketing Status: Discontinued
Patent and Exclusivity Information
GAVISCON (ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE)
Proprietary Name: GAVISCON
Dosage Form; Route of Administration: TABLET, CHEWABLE; ORAL
Strength: 80MG;20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N018685
Product Number: 001
Approval Date: Dec 9, 1983
Applicant Holder Full Name: CHATTEM INC DBA SANOFI CONSUMER HEALTHCARE
Marketing Status: Discontinued
Patent and Exclusivity Information
160MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE
Proprietary Name: GAVISCON
Dosage Form; Route of Administration: TABLET, CHEWABLE; ORAL
Strength: 160MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N018685
Product Number: 002
Approval Date: Dec 9, 1983
Applicant Holder Full Name: CHATTEM INC DBA SANOFI CONSUMER HEALTHCARE
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: GAVISCON
Dosage Form; Route of Administration: TABLET, CHEWABLE; ORAL
Strength: 160MG;40MG **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: N018685
Product Number: 002
Approval Date: Dec 9, 1983
Applicant Holder Full Name: CHATTEM INC DBA SANOFI CONSUMER HEALTHCARE
Marketing Status: Discontinued
Patent and Exclusivity Information