NDC 68788-6834

venlafaxine hydrochloride

Venlafaxine Hydrochloride

venlafaxine hydrochloride is a Oral Capsule, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Venlafaxine Hydrochloride.

Product ID68788-6834_0ab11627-3bf4-4344-aec8-f28b517fcefe
NDC68788-6834
Product TypeHuman Prescription Drug
Proprietary Namevenlafaxine hydrochloride
Generic NameVenlafaxine Hydrochloride
Dosage FormCapsule, Extended Release
Route of AdministrationORAL
Marketing Start Date2016-11-22
Marketing CategoryANDA / ANDA
Application NumberANDA090174
Labeler NamePreferred Pharmaceuticals Inc.
Substance NameVENLAFAXINE HYDROCHLORIDE
Active Ingredient Strength38 mg/1
Pharm ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 68788-6834-1

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6834-1)
Marketing Start Date2016-11-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-6834-2 [68788683402]

venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA090174
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-22

NDC 68788-6834-8 [68788683408]

venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA090174
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-22

NDC 68788-6834-3 [68788683403]

venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA090174
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-22

NDC 68788-6834-6 [68788683406]

venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA090174
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-11-22

NDC 68788-6834-1 [68788683401]

venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA090174
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-22

NDC 68788-6834-9 [68788683409]

venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA090174
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-22

Drug Details

Active Ingredients

IngredientStrength
VENLAFAXINE HYDROCHLORIDE37.5 mg/1

OpenFDA Data

SPL SET ID:875fe4d6-cf60-4043-ba5f-6180fe44a719
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 313583

    • Pharmacological Class

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

    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.