Venlafaxine
- Product NDC
- 0527-2606
- 11-digit product format
- 005272606
- Labeler code
- 0527
- Product ID
- 0527-2606_b296ebac-8124-4376-8b0b-3acd719df847
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA213927
- Marketing category
- ANDA
- Marketing start
- 2021-04-06
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0527-2606 | VENLAFAXINE TABLET [LANNETT COMPANY, INC.] | 4 | Legacy NDC | 20221231_5077a230-37f0-420f-a898-426496d795c6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0527-2606-32 | 00527260632 | 30 TABLET in 1 BOTTLE (0527-2606-32) | 30 tablet | 2021-05-01 | 0000-00-00 | No | No | Current |
| 0527-2606-46 | 00527260646 | 90 TABLET in 1 BOTTLE (0527-2606-46) | 90 tablet | 2021-05-01 | 0000-00-00 | No | No | Current |