Venlafaxine
- Product NDC
- 70518-3269
- 11-digit product format
- 705183269
- Labeler code
- 70518
- Product ID
- 70518-3269_d0fe474c-e991-73c2-e053-2a95a90abe8a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA213927
- Marketing category
- ANDA
- Marketing start
- 2021-11-16
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3269 | VENLAFAXINE TABLET [REMEDYREPACK INC.] | 1 | Legacy NDC | 20211118_5c93d0ec-f272-4f7b-8a05-7660ad5342f8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3269-0 | 70518326900 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3269-0) | 90 tablet | 2021-11-16 | 0000-00-00 | No | No | Current |