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 | 21695-045_8a2302ca-5c25-4d2d-9ffe-320080934aab |
NDC | 21695-045 |
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 | 38 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 |
Marketing Start Date | 1997-11-01 |
NDC Exclude Flag | N |
Sample Package? | N |
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 |
Ingredient | Strength |
---|---|
VENLAFAXINE HYDROCHLORIDE | 37.5 mg/1 |
SPL SET ID: | 8a2302ca-5c25-4d2d-9ffe-320080934aab |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
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 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EFFEXOR 98438579 not registered Live/Pending |
Viatris Specialty LLC 2024-03-07 |
EFFEXOR 74229208 1787331 Live/Registered |
WYETH LLC 1991-12-11 |