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venlafaxine hydrochloride
venlafaxine hydrochloride - 68382-034-10 - (venlafaxine hydrochloride)
Drug Information of venlafaxine hydrochloride
| Product NDC: | 68382-034 |
| 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: | 68382-034 |
| Labeler Name: | Zydus Pharmaceuticals (USA) Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090174 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110601 |
Package Information of venlafaxine hydrochloride
| Package NDC: | 68382-034-10 |
| Package Description: | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-10) |
NDC Information of venlafaxine hydrochloride
| NDC Code | 68382-034-10 |
| Proprietary Name | venlafaxine hydrochloride |
| Package Description | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-10) |
| Product NDC | 68382-034 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | venlafaxine hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110601 |
| Marketing Category Name | ANDA |
| Labeler Name | Zydus Pharmaceuticals (USA) Inc. |
| 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] |
