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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 074132

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NORTRIPTYLINE HYDROCHLORIDE (NORTRIPTYLINE HYDROCHLORIDE)
EQ 10MG BASE
Marketing Status: Prescription
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: AB
Application Number: A074132
Product Number: 001
Approval Date: Mar 27, 1995
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
NORTRIPTYLINE HYDROCHLORIDE (NORTRIPTYLINE HYDROCHLORIDE)
EQ 25MG BASE
Marketing Status: Prescription
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: AB
Application Number: A074132
Product Number: 002
Approval Date: Mar 27, 1995
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
NORTRIPTYLINE HYDROCHLORIDE (NORTRIPTYLINE HYDROCHLORIDE)
EQ 50MG BASE
Marketing Status: Prescription
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: AB
Application Number: A074132
Product Number: 003
Approval Date: Mar 27, 1995
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
NORTRIPTYLINE HYDROCHLORIDE (NORTRIPTYLINE HYDROCHLORIDE)
EQ 75MG BASE
Marketing Status: Prescription
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: AB
Application Number: A074132
Product Number: 004
Approval Date: Mar 27, 1995
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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