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VENLAFAXINE HYDROCHLORIDE
VENLAFAXINE HYDROCHLORIDE - 55648-716-02 - (VENLAFAXINE HYDROCHLORIDE)
Drug Information of VENLAFAXINE HYDROCHLORIDE
| Product NDC: | 55648-716 |
| Proprietary Name: | VENLAFAXINE HYDROCHLORIDE |
| Non Proprietary Name: | VENLAFAXINE HYDROCHLORIDE |
| Active Ingredient(s): | 37.5 mg/1 & nbsp; VENLAFAXINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VENLAFAXINE HYDROCHLORIDE
| Product NDC: | 55648-716 |
| Labeler Name: | WOCKHARDT LIMITED |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078865 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110414 |
Package Information of VENLAFAXINE HYDROCHLORIDE
| Package NDC: | 55648-716-02 |
| Package Description: | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55648-716-02) |
NDC Information of VENLAFAXINE HYDROCHLORIDE
| NDC Code | 55648-716-02 |
| Proprietary Name | VENLAFAXINE HYDROCHLORIDE |
| Package Description | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55648-716-02) |
| Product NDC | 55648-716 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | VENLAFAXINE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110414 |
| Marketing Category Name | ANDA |
| Labeler Name | WOCKHARDT LIMITED |
| Substance Name | VENLAFAXINE HYDROCHLORIDE |
| Strength Number | 37.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
