NDC 63629-3324

Venlafaxine

Venlafaxine

Venlafaxine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Venlafaxine Hydrochloride.

Product ID63629-3324_1c3e5c61-5e23-4230-bca5-ee1845f76d7a
NDC63629-3324
Product TypeHuman Prescription Drug
Proprietary NameVenlafaxine
Generic NameVenlafaxine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2008-06-13
Marketing CategoryANDA /
Application NumberANDA077653
Labeler NameBryant Ranch Prepack
Substance NameVENLAFAXINE HYDROCHLORIDE
Active Ingredient Strength75 mg/1
Pharm ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63629-3324-1

60 TABLET in 1 BOTTLE (63629-3324-1)
Marketing Start Date2022-07-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-3324-4 [63629332404]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA077653
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-06-13
Marketing End Date2017-08-30

NDC 63629-3324-2 [63629332402]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA077653
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-03-01
Marketing End Date2017-08-30

NDC 63629-3324-5 [63629332405]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA077653
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-06-13
Marketing End Date2017-08-30

NDC 63629-3324-3 [63629332403]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA077653
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-03-01
Marketing End Date2017-08-30

NDC 63629-3324-1 [63629332401]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA077653
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-03-01
Marketing End Date2017-08-30

NDC 63629-3324-6 [63629332406]

Venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA077653
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-06-13
Marketing End Date2017-08-30

Drug Details

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
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