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Venlafaxine Hydrochloride
Venlafaxine Hydrochloride - 59762-0182-3 - (VENLAFAXINE HYDROCHLORIDE)
Drug Information of Venlafaxine Hydrochloride
| Product NDC: | 59762-0182 |
| Proprietary Name: | Venlafaxine Hydrochloride |
| Non Proprietary Name: | VENLAFAXINE HYDROCHLORIDE |
| Active Ingredient(s): | 150 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: | 59762-0182 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020699 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20110602 |
Package Information of Venlafaxine Hydrochloride
| Package NDC: | 59762-0182-3 |
| Package Description: | 100 BLISTER PACK in 1 CARTON (59762-0182-3) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Venlafaxine Hydrochloride
| NDC Code | 59762-0182-3 |
| Proprietary Name | Venlafaxine Hydrochloride |
| Package Description | 100 BLISTER PACK in 1 CARTON (59762-0182-3) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 59762-0182 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | VENLAFAXINE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110602 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | VENLAFAXINE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
