NDC 67046-852

Venlafaxine

Venlafaxine

Venlafaxine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Contract Pharmacy Services-pa. The primary component is Venlafaxine Hydrochloride.

Product ID67046-852_64f0ff35-7f43-c84d-e053-2991aa0a1d22
NDC67046-852
Product TypeHuman Prescription Drug
Proprietary NameVenlafaxine
Generic NameVenlafaxine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-09-21
Marketing CategoryANDA / ANDA
Application NumberANDA078554
Labeler NameContract Pharmacy Services-PA
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 67046-852-60

60 TABLET in 1 BLISTER PACK (67046-852-60)
Marketing Start Date2017-09-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67046-852-28 [67046085228]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA078554
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-21
Inactivation Date2020-01-31

NDC 67046-852-07 [67046085207]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA078554
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-21
Inactivation Date2020-01-31

NDC 67046-852-21 [67046085221]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA078554
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-21
Inactivation Date2020-01-31

NDC 67046-852-60 [67046085260]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA078554
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-21
Inactivation Date2020-01-31

NDC 67046-852-20 [67046085220]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA078554
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-21
Inactivation Date2020-01-31

NDC 67046-852-14 [67046085214]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA078554
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-21
Inactivation Date2020-01-31

NDC 67046-852-30 [67046085230]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA078554
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-21
Inactivation Date2020-01-31

NDC 67046-852-15 [67046085215]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA078554
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-21
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
VENLAFAXINE HYDROCHLORIDE75 mg/1

OpenFDA Data

SPL SET ID:59b3e091-0464-1fd1-e053-2991aa0a5ecc
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 313586
    • UPC Code
  • 0323155249019

    • 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.