venlafaxine hydrochloride
- Product NDC
- 16714-045
- 11-digit product format
- 167140045
- Labeler code
- 16714
- Product ID
- 16714-045_522af844-d0ec-454e-8117-02528fb7cb33
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Northstar Rx LLC.
- Application
- ANDA090174
- Marketing category
- ANDA
- Marketing start
- 2021-06-10
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 150 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-045-01 | 16714004501 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-045-01) | 2021-06-10 | 0000-00-00 | No | No | Current |