NDC 0008-0837

Effexor XR

Venlafaxine Hydrochloride

Effexor XR is a Oral Capsule, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.. The primary component is Venlafaxine Hydrochloride.

• Product ID: 0008-0837_0a5ea9cc-56af-4474-a69e-443eed935fc8
• NDC: 0008-0837
• Product Type: Human Prescription Drug
• Proprietary Name: Effexor XR
• Generic Name: Venlafaxine Hydrochloride
• Dosage Form: Capsule, Extended Release
• Route of Administration: ORAL
• Marketing Start Date: 1997-11-01
• Marketing Category: NDA / NDA
• Application Number: NDA020699
• Labeler Name: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
• Substance Name: VENLAFAXINE HYDROCHLORIDE
• Active Ingredient Strength: 38 mg/1
• Pharm Classes: Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0008-0837-03

100 BLISTER PACK in 1 CARTON (0008-0837-03) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0008-0837-02)

• Marketing Start Date: 1997-11-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0008-0837-20 [00008083720]

Effexor XR CAPSULE, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA020699
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1997-11-01

NDC 0008-0837-21 [00008083721]

Effexor XR CAPSULE, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA020699
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1997-11-01

NDC 0008-0837-22 [00008083722]

Effexor XR CAPSULE, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA020699
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1997-11-01

NDC 0008-0837-03 [00008083703]

Effexor XR CAPSULE, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA020699
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1997-11-01

NDC 0008-0837-02 [00008083702]

Effexor XR CAPSULE, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA020699
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-09-30

Drug Details

Active Ingredients

Ingredient	Strength
VENLAFAXINE HYDROCHLORIDE	37.5 mg/1

OpenFDA Data

• SPL SET ID: 53c3e7ac-1852-4d70-d2b6-4fca819acf26
• Manufacturer:
  • Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
• UNII:
  • 7D7RX5A8MO
• RxNorm Concept Unique ID - RxCUI:
  • 729929
  • 729932
  • 729931
  • 313583
  • 313581
  • 313585
• UPC Code:
  • 0300080837207

Pharmacological Class

• Norepinephrine Uptake Inhibitors [MoA]
• Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
• Serotonin Uptake Inhibitors [MoA]

NDC Crossover Matching brand name "Effexor XR" or generic name "Venlafaxine Hydrochloride"

NDC	Brand Name	Generic Name
55289-277	Effexor XR	Effexor XR
70518-2156	Effexor XR	Effexor XR
70518-2157	Effexor XR	Effexor XR
80425-0088	Effexor XR	Effexor XR
0008-0833	Effexor	VENLAFAXINE HYDROCHLORIDE
0008-0836	Effexor	VENLAFAXINE HYDROCHLORIDE
0008-0837	Effexor	VENLAFAXINE HYDROCHLORIDE
0093-0199	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride
0093-7380	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride
0093-7381	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride
0093-7382	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride
0093-7383	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride
0093-7384	Venlafaxine Hydrochloride	Venlafaxine Hydrochloride