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:
Application Number: A206771
Product Number: 001
Approval Date: Jun 12, 2023
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
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:
Application Number: A206771
Product Number: 002
Approval Date: Jun 12, 2023
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information