Venlafaxine Hydrochloride
- Product NDC
- 42254-050
- 11-digit product format
- 422540050
- Labeler code
- 42254
- Product ID
- 42254-050_a4e1d3bc-4e97-4ff0-9e30-22a699c96072
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA077653
- Marketing category
- ANDA
- Marketing start
- 2008-06-13
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 42254-050-30 | Venlafaxine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 42254-050-60 | Venlafaxine Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42254-050 | VENLAFAXINE HYDROCHLORIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 2 package rows | 20120411_a4e1d3bc-4e97-4ff0-9e30-22a699c96072.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 42254-050-30 | 42254005030 | 30 in 1 BOTTLE | Historical |
| 42254-050-60 | 42254005060 | 60 in 1 BOTTLE | Historical |