Product Details for NDA 020699
EFFEXOR XR (VENLAFAXINE HYDROCHLORIDE)
EQ 37.5MG BASE
Marketing Status: Prescription
EQ 75MG BASE
Marketing Status: Prescription
EQ 150MG BASE
Marketing Status: Prescription
EQ 100MG BASE
Marketing Status: Discontinued
EQ 37.5MG BASE
Marketing Status: Prescription
Active Ingredient: VENLAFAXINE HYDROCHLORIDE
Proprietary Name: EFFEXOR XR
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: EQ 37.5MG BASE
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N020699
Product Number: 001
Approval Date: Oct 20, 1997
Applicant Holder Full Name: UPJOHN US 2 LLC
Marketing Status: Prescription
Patent and Exclusivity Information
EFFEXOR XR (VENLAFAXINE HYDROCHLORIDE)
Proprietary Name: EFFEXOR XR
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: EQ 37.5MG BASE
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N020699
Product Number: 001
Approval Date: Oct 20, 1997
Applicant Holder Full Name: UPJOHN US 2 LLC
Marketing Status: Prescription
Patent and Exclusivity Information
EQ 75MG BASE
Marketing Status: Prescription
Active Ingredient: VENLAFAXINE HYDROCHLORIDE
Proprietary Name: EFFEXOR XR
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: EQ 75MG BASE
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N020699
Product Number: 002
Approval Date: Oct 20, 1997
Applicant Holder Full Name: UPJOHN US 2 LLC
Marketing Status: Prescription
Patent and Exclusivity Information
EFFEXOR XR (VENLAFAXINE HYDROCHLORIDE)
Proprietary Name: EFFEXOR XR
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: EQ 75MG BASE
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N020699
Product Number: 002
Approval Date: Oct 20, 1997
Applicant Holder Full Name: UPJOHN US 2 LLC
Marketing Status: Prescription
Patent and Exclusivity Information
EQ 150MG BASE
Marketing Status: Prescription
Active Ingredient: VENLAFAXINE HYDROCHLORIDE
Proprietary Name: EFFEXOR XR
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: EQ 150MG BASE
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N020699
Product Number: 004
Approval Date: Oct 20, 1997
Applicant Holder Full Name: UPJOHN US 2 LLC
Marketing Status: Prescription
Patent and Exclusivity Information
EFFEXOR XR (VENLAFAXINE HYDROCHLORIDE)
Proprietary Name: EFFEXOR XR
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: EQ 150MG BASE
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N020699
Product Number: 004
Approval Date: Oct 20, 1997
Applicant Holder Full Name: UPJOHN US 2 LLC
Marketing Status: Prescription
Patent and Exclusivity Information
EQ 100MG BASE
Marketing Status: Discontinued
Active Ingredient: VENLAFAXINE HYDROCHLORIDE
Proprietary Name: EFFEXOR XR
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: EQ 100MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N020699
Product Number: 003
Approval Date: Oct 20, 1997
Applicant Holder Full Name: UPJOHN US 2 LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: EFFEXOR XR
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: EQ 100MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N020699
Product Number: 003
Approval Date: Oct 20, 1997
Applicant Holder Full Name: UPJOHN US 2 LLC
Marketing Status: Discontinued
Patent and Exclusivity Information