Venlafaxine Hydrochloride
- Product NDC
- 35356-375
- 11-digit product format
- 353560375
- Labeler code
- 35356
- Product ID
- 35356-375_a43036ed-d0de-430b-8c06-2400e6cdaced
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077653
- Marketing category
- ANDA
- Marketing start
- 2008-06-13
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 35356-375-30 | 2025-01-14 | C162847 | 48780-1 | ba0f9c33-5a3f-a910-e053-dadaa90a0b85 | 96c70a5e-8742-4530-8657-c82c82d64f17 |
| 35356-375-60 | 2025-01-14 | C162847 | 48780-1 | ba0f9c33-5a3f-a910-e053-dadaa90a0b85 | 96c70a5e-8742-4530-8657-c82c82d64f17 |
| 35356-375-90 | 2025-01-14 | C162847 | 48780-1 | ba0f9c33-5a3f-a910-e053-dadaa90a0b85 | 96c70a5e-8742-4530-8657-c82c82d64f17 |
| 35356-375-30 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-5a3f-a910-e053-dadaa90a0b85 | 96c70a5e-8742-4530-8657-c82c82d64f17 |
| 35356-375-60 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-5a3f-a910-e053-dadaa90a0b85 | 96c70a5e-8742-4530-8657-c82c82d64f17 |
| 35356-375-90 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-5a3f-a910-e053-dadaa90a0b85 | 96c70a5e-8742-4530-8657-c82c82d64f17 |