Venlafaxine
- Product NDC
- 53217-238
- 11-digit product format
- 532170238
- Labeler code
- 53217
- Product ID
- 53217-238_a5d860fb-40d9-422c-b330-0dbe8c018626
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA078627
- Marketing category
- ANDA
- Marketing start
- 2008-06-13
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 50 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53217-238-60 | Venlafaxine | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
| 53217-238-90 | Venlafaxine | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-238 | VENLAFAXINE TABLET [AIDAREX PHARMACEUTICALS LLC] | 3 | Legacy NDC, 2 package rows | 20161209_34734ecc-9b96-4a75-9418-1cc0401c2429.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-238-60 | 53217023860 | 60 in 1 BOTTLE | Historical |
| 53217-238-90 | 53217023890 | 90 in 1 BOTTLE | Historical |