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venlafaxine hydrochloride
venlafaxine hydrochloride - 65580-301-03 - (venlafaxine hydrochloride)
Drug Information of venlafaxine hydrochloride
| Product NDC: | 65580-301 |
| 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): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of venlafaxine hydrochloride
| Product NDC: | 65580-301 |
| Labeler Name: | Upstate Pharma, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022104 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080930 |
Package Information of venlafaxine hydrochloride
| Package NDC: | 65580-301-03 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65580-301-03) |
NDC Information of venlafaxine hydrochloride
| NDC Code | 65580-301-03 |
| Proprietary Name | venlafaxine hydrochloride |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65580-301-03) |
| Product NDC | 65580-301 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | venlafaxine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20080930 |
| Marketing Category Name | NDA |
| Labeler Name | Upstate Pharma, LLC |
| 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] |
