Product Details for ANDA 075185
DICLOFENAC SODIUM (DICLOFENAC SODIUM)
25MG
Marketing Status: Prescription
50MG
Marketing Status: Prescription
75MG
Marketing Status: Prescription
25MG
Marketing Status: Prescription
Active Ingredient: DICLOFENAC SODIUM
Proprietary Name: DICLOFENAC SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075185
Product Number: 002
Approval Date: Nov 13, 1998
Applicant Holder Full Name: CARLSBAD TECHNOLOGY INC
Marketing Status: Prescription
Patent and Exclusivity Information
DICLOFENAC SODIUM (DICLOFENAC SODIUM)
Proprietary Name: DICLOFENAC SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075185
Product Number: 002
Approval Date: Nov 13, 1998
Applicant Holder Full Name: CARLSBAD TECHNOLOGY INC
Marketing Status: Prescription
Patent and Exclusivity Information
50MG
Marketing Status: Prescription
Active Ingredient: DICLOFENAC SODIUM
Proprietary Name: DICLOFENAC SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075185
Product Number: 003
Approval Date: Nov 13, 1998
Applicant Holder Full Name: CARLSBAD TECHNOLOGY INC
Marketing Status: Prescription
Patent and Exclusivity Information
DICLOFENAC SODIUM (DICLOFENAC SODIUM)
Proprietary Name: DICLOFENAC SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075185
Product Number: 003
Approval Date: Nov 13, 1998
Applicant Holder Full Name: CARLSBAD TECHNOLOGY INC
Marketing Status: Prescription
Patent and Exclusivity Information
75MG
Marketing Status: Prescription
Active Ingredient: DICLOFENAC SODIUM
Proprietary Name: DICLOFENAC SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 75MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075185
Product Number: 001
Approval Date: Nov 13, 1998
Applicant Holder Full Name: CARLSBAD TECHNOLOGY INC
Marketing Status: Prescription
Patent and Exclusivity Information
Proprietary Name: DICLOFENAC SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 75MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075185
Product Number: 001
Approval Date: Nov 13, 1998
Applicant Holder Full Name: CARLSBAD TECHNOLOGY INC
Marketing Status: Prescription
Patent and Exclusivity Information