Venlafaxine Hydrochloride
- Product NDC
- 43353-234
- 11-digit product format
- 433530234
- Labeler code
- 43353
- Product ID
- 43353-234_c0d29c8f-bd6a-4b5c-adba-7e5ebdd8029c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA200834
- Marketing category
- ANDA
- Marketing start
- 2011-11-23
- 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
- 2020-12-31
- 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 |
|---|
| 43353-234 | VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC | 20171012_d004bcdd-5f1b-41fa-9bd8-966468d86d7d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43353-234-53 | 43353023453 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43353-234-53) | 2016-10-13 | 0000-00-00 | No | No | Current |
| 43353-234-79 | 43353023479 | 2160 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43353-234-79) | 2016-09-16 | 0000-00-00 | No | No | Current |