venlafaxine hydrochloride
- Product NDC
- 68788-6834
- 11-digit product format
- 687886834
- Labeler code
- 68788
- Product ID
- 68788-6834_56a0aeb6-55c1-4268-bf12-6eaa20766f5f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090174
- Marketing category
- ANDA
- Marketing start
- 2016-11-22
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 38 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 |
|---|
| 68788-6834-1 | 68788683401 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6834-1) | 2016-11-22 | 0000-00-00 | No | No | Current |
| 68788-6834-2 | 68788683402 | 20 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6834-2) | 2016-11-22 | 0000-00-00 | No | No | Current |
| 68788-6834-3 | 68788683403 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6834-3) | 2016-11-22 | 0000-00-00 | No | No | Current |
| 68788-6834-6 | 68788683406 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6834-6) | 2016-11-22 | 0000-00-00 | No | No | Current |
| 68788-6834-8 | 68788683408 | 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6834-8) | 2016-11-22 | 0000-00-00 | No | No | Current |
| 68788-6834-9 | 68788683409 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6834-9) | 2016-11-22 | 0000-00-00 | No | No | Current |