NDC 51079-482

Venlafaxine Hydrochloride

Venlafaxine Hydrochloride

Venlafaxine Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Mylan Institutional Inc.. The primary component is Venlafaxine Hydrochloride.

Product ID51079-482_7d8f4dae-c749-57cb-e053-2991aa0ab059
NDC51079-482
Product TypeHuman Prescription Drug
Proprietary NameVenlafaxine Hydrochloride
Generic NameVenlafaxine Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2008-07-15
Marketing CategoryANDA / ANDA
Application NumberANDA077166
Labeler NameMylan Institutional Inc.
Substance NameVENLAFAXINE HYDROCHLORIDE
Active Ingredient Strength75 mg/1
Pharm ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 51079-482-20

100 BLISTER PACK in 1 CARTON (51079-482-20) > 1 TABLET in 1 BLISTER PACK (51079-482-01)
Marketing Start Date2008-07-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51079-482-20 [51079048220]

Venlafaxine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA077166
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-07-15
Marketing End Date2020-12-31

NDC 51079-482-01 [51079048201]

Venlafaxine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA077166
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-07-15
Marketing End Date2020-12-31

NDC 51079-482-30 [51079048230]

Venlafaxine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA077166
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-07-15
Marketing End Date2020-12-31

NDC 51079-482-56 [51079048256]

Venlafaxine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA077166
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-01
Marketing End Date2018-12-31

Drug Details

Active Ingredients

IngredientStrength
VENLAFAXINE HYDROCHLORIDE75 mg/1

OpenFDA Data

SPL SET ID:6be70efb-322e-4e65-9851-a7d167065dd8
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 313586
  • 313584
  • Pharmacological Class

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

    Medicade Reported Pricing

    51079048256 VENLAFAXINE HCL 75 MG TABLET

    Pricing Unit: EA | Drug Type:

    51079048230 VENLAFAXINE HCL 75 MG TABLET

    Pricing Unit: EA | Drug Type:

    51079048220 VENLAFAXINE HCL 75 MG TABLET

    Pricing Unit: EA | Drug Type:

    51079048201 VENLAFAXINE HCL 75 MG TABLET

    Pricing Unit: EA | Drug Type:

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

    NDCBrand NameGeneric Name
    0093-0199Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0093-7380Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0093-7381Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0093-7382Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0093-7383Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0093-7384Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68025-081Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68025-079Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68071-1579VENLAFAXINE HYDROCHLORIDEVENLAFAXINE HYDROCHLORIDE
    68071-1673Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68025-080Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68025-082Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68071-1566venlafaxine hydrochloridevenlafaxine hydrochloride
    68071-4164venlafaxine hydrochloridevenlafaxine hydrochloride
    68071-4250Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68071-4442venlafaxine hydrochloridevenlafaxine hydrochloride
    68084-698Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68084-709Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68084-713Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68151-0308Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68151-3660Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68151-3659Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68382-034venlafaxine hydrochloridevenlafaxine hydrochloride
    68382-036venlafaxine hydrochloridevenlafaxine hydrochloride
    68382-035venlafaxine hydrochloridevenlafaxine hydrochloride
    68788-6424venlafaxine hydrochloridevenlafaxine hydrochloride
    68788-6806venlafaxine hydrochloridevenlafaxine hydrochloride
    68788-6834venlafaxine hydrochloridevenlafaxine hydrochloride
    68820-105Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68788-8917VENLAFAXINE HYDROCHLORIDEVENLAFAXINE HYDROCHLORIDE
    68820-106Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    68820-107Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    70518-0478venlafaxine hydrochloridevenlafaxine hydrochloride
    70518-0558venlafaxine hydrochloridevenlafaxine hydrochloride
    70518-0428Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    70518-0742venlafaxine hydrochloridevenlafaxine hydrochloride
    70518-1010venlafaxine hydrochloridevenlafaxine hydrochloride
    70518-0982Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    70518-1777Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    71335-0563Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    71335-0184venlafaxine hydrochloridevenlafaxine hydrochloride
    71610-013Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    71610-018Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0615-7622Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0615-7621Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0615-8122Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0904-6468Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0904-6246VENLAFAXINE HYDROCHLORIDEVENLAFAXINE HYDROCHLORIDE
    0904-6470Venlafaxine HydrochlorideVenlafaxine Hydrochloride
    0904-6469Venlafaxine HydrochlorideVenlafaxine Hydrochloride

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