Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 011856

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SOLU-MEDROL (METHYLPREDNISOLONE SODIUM SUCCINATE)
EQ 40MG BASE/VIAL
Marketing Status: Prescription
Active Ingredient: METHYLPREDNISOLONE SODIUM SUCCINATE
Proprietary Name: SOLU-MEDROL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 40MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N011856
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status:  Prescription
Patent and Exclusivity Information
SOLU-MEDROL (METHYLPREDNISOLONE SODIUM SUCCINATE)
EQ 125MG BASE/VIAL
Marketing Status: Prescription
Active Ingredient: METHYLPREDNISOLONE SODIUM SUCCINATE
Proprietary Name: SOLU-MEDROL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 125MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N011856
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status:  Prescription
Patent and Exclusivity Information
SOLU-MEDROL (METHYLPREDNISOLONE SODIUM SUCCINATE)
EQ 500MG BASE/VIAL
Marketing Status: Prescription
Active Ingredient: METHYLPREDNISOLONE SODIUM SUCCINATE
Proprietary Name: SOLU-MEDROL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N011856
Product Number: 005
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status:  Prescription
Patent and Exclusivity Information
SOLU-MEDROL (METHYLPREDNISOLONE SODIUM SUCCINATE)
EQ 1GM BASE/VIAL
Marketing Status: Prescription
Active Ingredient: METHYLPREDNISOLONE SODIUM SUCCINATE
Proprietary Name: SOLU-MEDROL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N011856
Product Number: 006
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status:  Prescription
Patent and Exclusivity Information
SOLU-MEDROL (METHYLPREDNISOLONE SODIUM SUCCINATE)
EQ 2GM BASE/VIAL
Marketing Status: Prescription
Active Ingredient: METHYLPREDNISOLONE SODIUM SUCCINATE
Proprietary Name: SOLU-MEDROL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N011856
Product Number: 007
Approval Date: Feb 27, 1985
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status:  Prescription
Patent and Exclusivity Information

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