Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 080350

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PREDNISONE (PREDNISONE)
1MG
Marketing Status: Discontinued
Active Ingredient: PREDNISONE
Proprietary Name: PREDNISONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A080350
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PANRAY CORP SUB ORMONT DRUG AND CHEMICAL CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
PREDNISONE (PREDNISONE)
2.5MG
Marketing Status: Discontinued
Active Ingredient: PREDNISONE
Proprietary Name: PREDNISONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A080350
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PANRAY CORP SUB ORMONT DRUG AND CHEMICAL CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
PREDNISONE (PREDNISONE)
5MG
Marketing Status: Discontinued
Active Ingredient: PREDNISONE
Proprietary Name: PREDNISONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A080350
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PANRAY CORP SUB ORMONT DRUG AND CHEMICAL CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

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