NDC 60760-187

venlafaxine

Venlafaxine Hydrochloride

venlafaxine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by St. Mary's Medical Park Pharmacy. The primary component is Venlafaxine Hydrochloride.

Product ID60760-187_8a1e6dab-5331-1ea4-e053-2a95a90a0e40
NDC60760-187
Product TypeHuman Prescription Drug
Proprietary Namevenlafaxine
Generic NameVenlafaxine Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2019-05-29
Marketing CategoryANDA / ANDA
Application NumberANDA090555
Labeler NameSt. Mary's Medical Park Pharmacy
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 Through2020-12-31

Packaging

NDC 60760-187-60

60 TABLET in 1 BOTTLE, PLASTIC (60760-187-60)
Marketing Start Date2019-05-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60760-187-60 [60760018760]

venlafaxine TABLET
Marketing CategoryANDA
Application NumberANDA090555
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-05-29

Drug Details

Active Ingredients

IngredientStrength
VENLAFAXINE HYDROCHLORIDE37.5 mg/1

Pharmacological Class

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

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

NDCBrand NameGeneric Name
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
71335-0942venlafaxinevenlafaxine
71335-0383VenlafaxineVenlafaxine
71335-0778venlafaxinevenlafaxine
0615-6567VenlafaxineVenlafaxine
0615-6566VenlafaxineVenlafaxine
0615-7557VenlafaxineVenlafaxine
0615-7558VenlafaxineVenlafaxine
16714-311venlafaxinevenlafaxine
16714-314venlafaxinevenlafaxine
16714-312venlafaxinevenlafaxine
16714-315venlafaxinevenlafaxine
16714-657VenlafaxineVenlafaxine
16714-658VenlafaxineVenlafaxine
16714-659VenlafaxineVenlafaxine
16714-656VenlafaxineVenlafaxine
16714-313venlafaxinevenlafaxine
16714-655VenlafaxineVenlafaxine
23155-249VenlafaxineVenlafaxine
23155-247VenlafaxineVenlafaxine
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.