Venlafaxine Hydrochloride
- Product NDC
- 0904-6470
- 11-digit product format
- 009046470
- Labeler code
- 0904
- Product ID
- 0904-6470_2f13e60d-a9f8-472c-b7b1-25c7805143af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA090899
- Marketing category
- ANDA
- Marketing start
- 2015-04-06
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 150 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6470-61 | 00904647061 | 100 BLISTER PACK in 1 CARTON (0904-6470-61) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK | 100 blister pack | 2015-04-06 | 0000-00-00 | No | No | Current |