Product Details for NDA 017371
PRONESTYL (PROCAINAMIDE HYDROCHLORIDE)
250MG
Marketing Status: Discontinued
375MG
Marketing Status: Discontinued
500MG
Marketing Status: Discontinued
250MG
Marketing Status: Discontinued
Active Ingredient: PROCAINAMIDE HYDROCHLORIDE
Proprietary Name: PRONESTYL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017371
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: APOTHECON INC DIV BRISTOL MYERS SQUIBB
Marketing Status: Discontinued
Patent and Exclusivity Information
PRONESTYL (PROCAINAMIDE HYDROCHLORIDE)
Proprietary Name: PRONESTYL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017371
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: APOTHECON INC DIV BRISTOL MYERS SQUIBB
Marketing Status: Discontinued
Patent and Exclusivity Information
375MG
Marketing Status: Discontinued
Active Ingredient: PROCAINAMIDE HYDROCHLORIDE
Proprietary Name: PRONESTYL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 375MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017371
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: APOTHECON INC DIV BRISTOL MYERS SQUIBB
Marketing Status: Discontinued
Patent and Exclusivity Information
PRONESTYL (PROCAINAMIDE HYDROCHLORIDE)
Proprietary Name: PRONESTYL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 375MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017371
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: APOTHECON INC DIV BRISTOL MYERS SQUIBB
Marketing Status: Discontinued
Patent and Exclusivity Information
500MG
Marketing Status: Discontinued
Active Ingredient: PROCAINAMIDE HYDROCHLORIDE
Proprietary Name: PRONESTYL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017371
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: APOTHECON INC DIV BRISTOL MYERS SQUIBB
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: PRONESTYL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017371
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: APOTHECON INC DIV BRISTOL MYERS SQUIBB
Marketing Status: Discontinued
Patent and Exclusivity Information