Home
>
National Drug Code (NDC)
>
Venlafaxine Hydrochloride
Venlafaxine Hydrochloride - 51079-135-20 - (venlafaxine)
Drug Information of Venlafaxine Hydrochloride
| Product NDC: | 51079-135 |
| Proprietary Name: | Venlafaxine Hydrochloride |
| Non Proprietary Name: | venlafaxine |
| Active Ingredient(s): | 75 mg/1 & nbsp; venlafaxine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Venlafaxine Hydrochloride
| Product NDC: | 51079-135 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078789 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110725 |
Package Information of Venlafaxine Hydrochloride
| Package NDC: | 51079-135-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-135-20) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (51079-135-01) |
NDC Information of Venlafaxine Hydrochloride
| NDC Code | 51079-135-20 |
| Proprietary Name | Venlafaxine Hydrochloride |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-135-20) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (51079-135-01) |
| Product NDC | 51079-135 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | venlafaxine |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110725 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | VENLAFAXINE HYDROCHLORIDE |
| Strength Number | 75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
