Venlafaxine Hydrochloride
- Product NDC
- 68071-2427
- 11-digit product format
- 680712427
- Labeler code
- 68071
- Product ID
- 68071-2427_d2915d53-132e-7215-e053-2a95a90a3624
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA212277
- Marketing category
- ANDA
- Marketing start
- 2019-07-08
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 150 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 |
|---|
| 68071-2427 | VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NUCARE PHARMACEUTICALS,INC.] | 3 | Legacy NDC | 20230718_c3694d1b-e858-5b9b-e053-2a95a90a346a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2427-9 | 68071242709 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-2427-9) | 2021-05-28 | 0000-00-00 | No | No | Current |