NDC 64725-0036

venlafaxine hydrochloride 150 mg capsule, extended release

On the label: TYA Pharmaceuticals. It's repackaged: TYA Pharmaceuticals rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-036.

Where the pills inside were made

Repackaging site

• TYA Pharmaceuticals, Location not on file · repackages it and relabels it

Recalls

• Jun 21, 2024 · Class II · Zydus Pharmaceuticals (USA) Inc
  Failed Dissolution Specifications: Out-of-specification results observed for dissolution testing at the 8-hour and 12-hour pull intervals.
  Lots: Lot #: a) M213175, Exp. Date 09/2024; b) M213176, Exp. Date 09/2024
• Jul 19, 2016 · Class II · Zydus Pharmaceuticals USA Inc
  Failed Dissolution Specifications: out of specification dissolution results in retained samples
  Lots: Lot #: a) MR10518, Exp. 9/2017; MR11051, MR11052, MR11053, MR11054, Exp. 10/2017; MR11403, Exp. 11/2017. Lot #: b) MR10197, MR10195, Exp. 09/2017; MR11482, Exp.10/2017; MR11479, MR11480, MR11481, MR11483, MR11665 Exp. 11/2017. Lot #: c) MR10404, MR10406, MR10521, Exp. 09/2017; MR10744, MR1105…
• Jul 19, 2016 · Class II · Zydus Pharmaceuticals USA Inc
  Failed Dissolution Specifications: out of specification dissolution results in retained samples
  Lots: Lot #: a) MS1217, MS1218 , Exp.12/2017. Lot #: b) MS1215, Exp.12/2017 Lot #: c) MR11150, MR11151, MR11854, Exp. 10/2017; MR11798, MR11799, MS1214, Exp.11/2017

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Venlafaxine: every company that makes it

Form

capsule, extended release

Strength

150 mg

Approval

ANDA ANDA090174

On the market since

Jun 1, 2011

Package NDCs

64725-0036-1

Official label

DailyMed (National Library of Medicine), updated Jul 11, 2014

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