Product Details for NDA 011757
DEPO-MEDROL (METHYLPREDNISOLONE ACETATE)
20MG/ML
Marketing Status: Prescription
40MG/ML
Marketing Status: Prescription
80MG/ML
Marketing Status: Prescription
20MG/ML
Marketing Status: Prescription
Active Ingredient: METHYLPREDNISOLONE ACETATE
Proprietary Name: DEPO-MEDROL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N011757
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status: Prescription
Patent and Exclusivity Information
DEPO-MEDROL (METHYLPREDNISOLONE ACETATE)
Proprietary Name: DEPO-MEDROL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N011757
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status: Prescription
Patent and Exclusivity Information
40MG/ML
Marketing Status: Prescription
Active Ingredient: METHYLPREDNISOLONE ACETATE
Proprietary Name: DEPO-MEDROL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 40MG/ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N011757
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status: Prescription
Patent and Exclusivity Information
DEPO-MEDROL (METHYLPREDNISOLONE ACETATE)
Proprietary Name: DEPO-MEDROL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 40MG/ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N011757
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status: Prescription
Patent and Exclusivity Information
80MG/ML
Marketing Status: Prescription
Active Ingredient: METHYLPREDNISOLONE ACETATE
Proprietary Name: DEPO-MEDROL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 80MG/ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N011757
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status: Prescription
Patent and Exclusivity Information
Proprietary Name: DEPO-MEDROL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 80MG/ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N011757
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status: Prescription
Patent and Exclusivity Information