Venlafaxine Hydrochloride
- Product NDC
- 50090-6215
- 11-digit product format
- 500906215
- Labeler code
- 50090
- Product ID
- 50090-6215_09f4b40e-ab85-435d-9331-94a30e732a38
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076565
- Marketing category
- ANDA
- Marketing start
- 2010-07-01
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 50090-6215-0 | Venlafaxine Hydrochloride | 29 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 29 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6215 | VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 1 package rows | 20221119_27656716-8525-4a3a-a110-a48f0c081c31.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 |
|---|
| 50090-6215-0 | 50090621500 | 29 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6215-0) | 2022-11-09 | 0000-00-00 | No | No | Current |