Venlafaxine Hydrochloride
- Product NDC
- 29033-046
- 11-digit product format
- 290330046
- Labeler code
- 29033
- Product ID
- 29033-046_11ed7ee6-1687-4eab-88fd-22fee419a846
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Nostrum Laboratories, Inc.
- Application
- ANDA205468
- Marketing category
- ANDA
- Marketing start
- 2017-03-27
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 225 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 |
|---|
| 29033-046-30 | Venlafaxine Hydrochloride | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | | 5 |
| 29033-046-90 | Venlafaxine Hydrochloride | 90 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 90 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 29033-046 | VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [NOSTRUM LABORATORIES, INC.] | 5 | Legacy NDC, 2 package rows | 20210610_b84c7126-9216-4f35-ace4-156a493e2b2d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 29033-046-30 | 29033004630 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (29033-046-30) | 2017-03-27 | 0000-00-00 | No | No | Current |
| 29033-046-90 | 29033004690 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (29033-046-90) | 2017-03-27 | 0000-00-00 | No | No | Current |