Product Details for NDA 207233
VIVLODEX (MELOXICAM)
5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: MELOXICAM
Proprietary Name: VIVLODEX
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N207233
Product Number: 001
Approval Date: Oct 22, 2015
Applicant Holder Full Name: ICEUTICA OPERATIONS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
VIVLODEX (MELOXICAM)
Proprietary Name: VIVLODEX
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N207233
Product Number: 001
Approval Date: Oct 22, 2015
Applicant Holder Full Name: ICEUTICA OPERATIONS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: MELOXICAM
Proprietary Name: VIVLODEX
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N207233
Product Number: 002
Approval Date: Oct 22, 2015
Applicant Holder Full Name: ICEUTICA OPERATIONS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: VIVLODEX
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: N207233
Product Number: 002
Approval Date: Oct 22, 2015
Applicant Holder Full Name: ICEUTICA OPERATIONS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information