Active Ingredient: DICLOFENAC SODIUM; MISOPROSTOL
Proprietary Name: DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 50MG;0.2MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A204355
Product Number: 001
Approval Date: Jul 15, 2021
Applicant Holder Full Name: MICRO LABS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: DICLOFENAC SODIUM; MISOPROSTOL
Proprietary Name: DICLOFENAC SODIUM AND MISOPROSTOL
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: 75MG;0.2MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A204355
Product Number: 002
Approval Date: Jul 15, 2021
Applicant Holder Full Name: MICRO LABS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information