venlafaxine
- Product NDC
- 68071-4341
- 11-digit product format
- 680714341
- Labeler code
- 68071
- Product ID
- 68071-4341_d60cf113-4ae5-4ae7-e053-2995a90ae9b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078932
- Marketing category
- ANDA
- Marketing start
- 2015-10-01
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4341-3 | 68071434103 | 30 TABLET in 1 BOTTLE (68071-4341-3) | 30 tablet | 2018-03-20 | 0000-00-00 | No | No | Current |
| 68071-4341-6 | 68071434106 | 60 TABLET in 1 BOTTLE (68071-4341-6) | 60 tablet | 2018-03-20 | 0000-00-00 | No | No | Current |
| 68071-4341-9 | 68071434109 | 90 TABLET in 1 BOTTLE (68071-4341-9) | 90 tablet | 2018-03-20 | 0000-00-00 | No | No | Current |