Product Details for ANDA 074054
NORTRIPTYLINE HYDROCHLORIDE (NORTRIPTYLINE HYDROCHLORIDE)
EQ 10MG BASE
Marketing Status: Discontinued
EQ 25MG BASE
Marketing Status: Discontinued
EQ 50MG BASE
Marketing Status: Discontinued
EQ 75MG BASE
Marketing Status: Discontinued
EQ 10MG BASE
Marketing Status: Discontinued
Active Ingredient: NORTRIPTYLINE HYDROCHLORIDE
Proprietary Name: NORTRIPTYLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074054
Product Number: 001
Approval Date: Dec 31, 1992
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
NORTRIPTYLINE HYDROCHLORIDE (NORTRIPTYLINE HYDROCHLORIDE)
Proprietary Name: NORTRIPTYLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074054
Product Number: 001
Approval Date: Dec 31, 1992
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 25MG BASE
Marketing Status: Discontinued
Active Ingredient: NORTRIPTYLINE HYDROCHLORIDE
Proprietary Name: NORTRIPTYLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 25MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074054
Product Number: 002
Approval Date: Dec 31, 1992
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
NORTRIPTYLINE HYDROCHLORIDE (NORTRIPTYLINE HYDROCHLORIDE)
Proprietary Name: NORTRIPTYLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 25MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074054
Product Number: 002
Approval Date: Dec 31, 1992
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 50MG BASE
Marketing Status: Discontinued
Active Ingredient: NORTRIPTYLINE HYDROCHLORIDE
Proprietary Name: NORTRIPTYLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 50MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074054
Product Number: 003
Approval Date: Dec 31, 1992
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
NORTRIPTYLINE HYDROCHLORIDE (NORTRIPTYLINE HYDROCHLORIDE)
Proprietary Name: NORTRIPTYLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 50MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074054
Product Number: 003
Approval Date: Dec 31, 1992
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 75MG BASE
Marketing Status: Discontinued
Active Ingredient: NORTRIPTYLINE HYDROCHLORIDE
Proprietary Name: NORTRIPTYLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 75MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074054
Product Number: 004
Approval Date: Dec 31, 1992
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: NORTRIPTYLINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 75MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074054
Product Number: 004
Approval Date: Dec 31, 1992
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status: Discontinued
Patent and Exclusivity Information