venlafaxine hydrochloride
- Product NDC
- 50090-2894
- 11-digit product format
- 500902894
- Labeler code
- 50090
- Product ID
- 50090-2894_2cf6905b-c0b5-435f-8785-df0f74de980f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090174
- Marketing category
- ANDA
- Marketing start
- 2011-06-01
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 75 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2894-0 | venlafaxine hydrochloride | 1 in 1 BLISTER PACK | CAPSULE, EXTENDED RELEASE | 1 | | 18 |
| 50090-2894-0 | venlafaxine hydrochloride | 29 in 1 BOX, UNIT-DOSE | CAPSULE, EXTENDED RELEASE | 29 | | 18 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2894 | VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS] | 18 | Legacy NDC, 2 package rows | 20210818_b49a550b-cd80-4e24-9ae9-52d362e36bdf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2894-0 | 50090289400 | 1 in 1 BLISTER PACK | Historical |