Venlafaxine Hydrochloride
- Product NDC
- 0179-0162
- 11-digit product format
- 001790162
- Labeler code
- 0179
- Product ID
- 0179-0162_7c4f4dbc-8117-41fa-e053-2a91aa0a7deb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA200834
- Marketing category
- ANDA
- Marketing start
- 2014-10-27
- Marketing end
- 2020-09-30
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record