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Venlafaxine hydrochloride
Venlafaxine hydrochloride - 64455-106-90 - (Venlafaxine hydrochloride)
Drug Information of Venlafaxine hydrochloride
| Product NDC: | 64455-106 |
| 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: | 64455-106 |
| Labeler Name: | BTA Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090071 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130101 |
Package Information of Venlafaxine hydrochloride
| Package NDC: | 64455-106-90 |
| Package Description: | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (64455-106-90) |
NDC Information of Venlafaxine hydrochloride
| NDC Code | 64455-106-90 |
| Proprietary Name | Venlafaxine hydrochloride |
| Package Description | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (64455-106-90) |
| Product NDC | 64455-106 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Venlafaxine hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | ANDA |
| Labeler Name | BTA Pharmaceuticals |
| 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] |
