Product Details for NDA 019516
MS CONTIN (MORPHINE SULFATE)
15MG
Marketing Status: Prescription
30MG
Marketing Status: Prescription
60MG
Marketing Status: Prescription
100MG
Marketing Status: Prescription
200MG
Marketing Status: Prescription
15MG
Marketing Status: Prescription
Active Ingredient: MORPHINE SULFATE
Proprietary Name: MS CONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 15MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N019516
Product Number: 003
Approval Date: Sep 12, 1989
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status: Prescription
Patent and Exclusivity Information
MS CONTIN (MORPHINE SULFATE)
Proprietary Name: MS CONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 15MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N019516
Product Number: 003
Approval Date: Sep 12, 1989
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status: Prescription
Patent and Exclusivity Information
30MG
Marketing Status: Prescription
Active Ingredient: MORPHINE SULFATE
Proprietary Name: MS CONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 30MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N019516
Product Number: 001
Approval Date: May 29, 1987
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status: Prescription
Patent and Exclusivity Information
MS CONTIN (MORPHINE SULFATE)
Proprietary Name: MS CONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 30MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N019516
Product Number: 001
Approval Date: May 29, 1987
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status: Prescription
Patent and Exclusivity Information
60MG
Marketing Status: Prescription
Active Ingredient: MORPHINE SULFATE
Proprietary Name: MS CONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 60MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N019516
Product Number: 002
Approval Date: Apr 8, 1988
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status: Prescription
Patent and Exclusivity Information
MS CONTIN (MORPHINE SULFATE)
Proprietary Name: MS CONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 60MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N019516
Product Number: 002
Approval Date: Apr 8, 1988
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status: Prescription
Patent and Exclusivity Information
100MG
Marketing Status: Prescription
Active Ingredient: MORPHINE SULFATE
Proprietary Name: MS CONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 100MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N019516
Product Number: 004
Approval Date: Jan 16, 1990
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status: Prescription
Patent and Exclusivity Information
MS CONTIN (MORPHINE SULFATE)
Proprietary Name: MS CONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 100MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N019516
Product Number: 004
Approval Date: Jan 16, 1990
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status: Prescription
Patent and Exclusivity Information
200MG
Marketing Status: Prescription
Active Ingredient: MORPHINE SULFATE
Proprietary Name: MS CONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 200MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N019516
Product Number: 005
Approval Date: Nov 8, 1993
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status: Prescription
Patent and Exclusivity Information
Proprietary Name: MS CONTIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 200MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N019516
Product Number: 005
Approval Date: Nov 8, 1993
Applicant Holder Full Name: PURDUE PHARMA LP
Marketing Status: Prescription
Patent and Exclusivity Information