Venlafaxine Hydrochloride
- Product NDC
- 50090-4854
- 11-digit product format
- 500904854
- Labeler code
- 50090
- Product ID
- 50090-4854_2e7031bb-a70f-4e76-b1bd-312e2dcddf3b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076690
- Marketing category
- ANDA
- Marketing start
- 2006-08-04
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 38 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
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 |
|---|
| 50090-4854-0 | Venlafaxine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 5 |
| 50090-4854-1 | Venlafaxine Hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4854 | VENLAFAXINE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 5 | Legacy NDC, 2 package rows | 20210416_4d1f5746-7179-4a68-b600-2940d7bf1915.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4854-0 | 50090485400 | 30 TABLET in 1 BOTTLE (50090-4854-0) | 30 tablet | 2020-01-21 | 0000-00-00 | No | No | Current |
| 50090-4854-1 | 50090485401 | 90 TABLET in 1 BOTTLE (50090-4854-1) | 90 tablet | 2020-01-21 | 0000-00-00 | No | No | Current |