NDC 61919-657

VENLAFAXINE

Venlafaxine

VENLAFAXINE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Direct Rx. The primary component is Venlafaxine Hydrochloride.

Product ID61919-657_3f4d6712-d471-5c1a-e054-00144ff88e88
NDC61919-657
Product TypeHuman Prescription Drug
Proprietary NameVENLAFAXINE
Generic NameVenlafaxine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2014-01-01
Marketing CategoryANDA / ANDA
Application NumberANDA078554
Labeler NameDIRECT RX
Substance NameVENLAFAXINE HYDROCHLORIDE
Active Ingredient Strength50 mg/1
Pharm ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 61919-657-30

30 TABLET in 1 BOTTLE (61919-657-30)
Marketing Start Date2014-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 61919-657-30 [61919065730]

VENLAFAXINE TABLET
Marketing CategoryANDA
Application NumberANDA078554
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-01-01

Drug Details

Active Ingredients

IngredientStrength
VENLAFAXINE HYDROCHLORIDE50 mg/1

OpenFDA Data

SPL SET ID:1ddeb8b8-e8af-4075-958d-7be6ce71f7df
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 314277
  • Pharmacological Class

    • Norepinephrine Uptake Inhibitors [MoA]
    • Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
    • Serotonin Uptake Inhibitors [MoA]

    NDC Crossover Matching brand name "VENLAFAXINE" or generic name "Venlafaxine"

    NDCBrand NameGeneric Name
    0527-2606VenlafaxineVenlafaxine
    0527-2616VenlafaxineVenlafaxine
    0615-6566VenlafaxineVenlafaxine
    0615-6567VenlafaxineVenlafaxine
    0615-7557VenlafaxineVenlafaxine
    0615-7558VenlafaxineVenlafaxine
    16714-311venlafaxinevenlafaxine
    16714-312venlafaxinevenlafaxine
    16714-313venlafaxinevenlafaxine
    16714-314venlafaxinevenlafaxine
    16714-315venlafaxinevenlafaxine
    16714-655VenlafaxineVenlafaxine
    16714-656VenlafaxineVenlafaxine
    16714-657VenlafaxineVenlafaxine
    16714-658VenlafaxineVenlafaxine
    16714-659VenlafaxineVenlafaxine
    23155-246VENLAFAXINEVENLAFAXINE
    23155-247VENLAFAXINEVENLAFAXINE
    23155-248VENLAFAXINEVENLAFAXINE
    68001-157VenlafaxineVenlafaxine
    68001-158VenlafaxineVenlafaxine
    68001-159VenlafaxineVenlafaxine
    68001-160VenlafaxineVenlafaxine
    68001-156VenlafaxineVenlafaxine
    68071-3286VenlafaxineVenlafaxine
    68071-2139VenlafaxineVenlafaxine
    68071-4341venlafaxinevenlafaxine
    68084-844VenlafaxineVenlafaxine
    68084-905VenlafaxineVenlafaxine
    68084-896VenlafaxineVenlafaxine
    68084-856VenlafaxineVenlafaxine
    68382-021VenlafaxineVenlafaxine
    68382-018VenlafaxineVenlafaxine
    68382-020VenlafaxineVenlafaxine
    68382-019VenlafaxineVenlafaxine
    68382-101VenlafaxineVenlafaxine
    70518-1245venlafaxinevenlafaxine
    70518-1976venlafaxinevenlafaxine
    70518-1228venlafaxinevenlafaxine
    70518-1547VenlafaxineVenlafaxine
    70518-1385venlafaxinevenlafaxine
    70518-1907venlafaxinevenlafaxine
    70518-1609VenlafaxineVenlafaxine
    71209-027VENLAFAXINEVENLAFAXINE
    71209-026VENLAFAXINEVENLAFAXINE
    71209-025VENLAFAXINEVENLAFAXINE
    71209-028VENLAFAXINEVENLAFAXINE
    71335-0106VenlafaxineVenlafaxine
    71335-0185VenlafaxineVenlafaxine
    71209-029VENLAFAXINEVENLAFAXINE

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.