venlafaxine hydrochloride
- Product NDC
- 35356-791
- 11-digit product format
- 353560791
- Labeler code
- 35356
- Product ID
- 35356-791_f1b48042-7d1d-4b02-a4a1-8247cc366b3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA090174
- Marketing category
- ANDA
- Marketing start
- 2011-06-01
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 38 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
- 2020-12-31
- 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 |
|---|
| 35356-791-30 | 35356079130 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (35356-791-30) | 2011-06-01 | 0000-00-00 | No | No | Current |
| 35356-791-60 | 35356079160 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (35356-791-60) | 2011-06-01 | 0000-00-00 | No | No | Current |