NDC 21695-046

Effexor XR Extended-Release

Venlafaxine Hydrochloride

Effexor XR Extended-Release is a Oral Capsule, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Rebel Distributors Corp. The primary component is Venlafaxine Hydrochloride.

• Product ID: 21695-046_8a2302ca-5c25-4d2d-9ffe-320080934aab
• NDC: 21695-046
• Product Type: Human Prescription Drug
• Proprietary Name: Effexor XR Extended-Release
• 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: Rebel Distributors Corp
• Substance Name: VENLAFAXINE HYDROCHLORIDE
• Active Ingredient Strength: 75 mg/1
• Pharm Classes: Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 21695-046-90

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (21695-046-90)

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

NDC SPL Data Element Entries

NDC 21695-046-30 [21695004630]

Effexor XR Extended-Release CAPSULE, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA020699
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1997-11-01
• Inactivation Date: 2019-09-24

NDC 21695-046-15 [21695004615]

Effexor XR Extended-Release CAPSULE, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA020699
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1997-11-01
• Inactivation Date: 2019-09-24

NDC 21695-046-90 [21695004690]

Effexor XR Extended-Release CAPSULE, EXTENDED RELEASE

• Marketing Category: NDA
• Application Number: NDA020699
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1997-11-01
• Inactivation Date: 2019-09-24

Drug Details

Active Ingredients

Ingredient	Strength
VENLAFAXINE HYDROCHLORIDE	75 mg/1

OpenFDA Data

• SPL SET ID: 8a2302ca-5c25-4d2d-9ffe-320080934aab
• Manufacturer:
  • Rebel Distributors Corp
• UNII:
  • 7D7RX5A8MO
• RxNorm Concept Unique ID - RxCUI:
  • 729929
  • 729932
  • 729931
  • 313583
  • 313581
  • 313585

Pharmacological Class

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

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

NDC	Brand Name	Generic Name
21695-047	Effexor XR Extended-Release	Effexor XR Extended-Release
21695-046	Effexor XR Extended-Release	Effexor XR Extended-Release
21695-045	Effexor XR Extended-Release	Effexor XR Extended-Release
67544-189	Effexor XR Extended-Release	Effexor XR Extended-Release
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