Product Details for NDA 006811
PARASAL SODIUM (AMINOSALICYLATE SODIUM)
500MG
Marketing Status: Discontinued
1GM
Marketing Status: Discontinued
500MG
Marketing Status: Discontinued
1GM
Marketing Status: Discontinued
500MG
Marketing Status: Discontinued
Active Ingredient: AMINOSALICYLATE SODIUM
Proprietary Name: PARASAL SODIUM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N006811
Product Number: 006
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
PARASAL SODIUM (AMINOSALICYLATE SODIUM)
Proprietary Name: PARASAL SODIUM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N006811
Product Number: 006
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
1GM
Marketing Status: Discontinued
Active Ingredient: AMINOSALICYLATE SODIUM
Proprietary Name: PARASAL SODIUM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1GM
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N006811
Product Number: 011
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
PARASAL (AMINOSALICYLIC ACID)
Proprietary Name: PARASAL SODIUM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1GM
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N006811
Product Number: 011
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
500MG
Marketing Status: Discontinued
Active Ingredient: AMINOSALICYLIC ACID
Proprietary Name: PARASAL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N006811
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
PARASAL (AMINOSALICYLIC ACID)
Proprietary Name: PARASAL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N006811
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
1GM
Marketing Status: Discontinued
Active Ingredient: AMINOSALICYLIC ACID
Proprietary Name: PARASAL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1GM
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N006811
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
Proprietary Name: PARASAL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1GM
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N006811
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