venlafaxine hydrochloride
- Product NDC
- 0904-7076
- 11-digit product format
- 009047076
- Labeler code
- 0904
- Product ID
- 0904-7076_ff1ddeb2-9129-4c02-9757-964662dcd0ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA090174
- Marketing category
- ANDA
- Marketing start
- 2011-06-01
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7076 | VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [MAJOR PHARMACEUTICALS] | 4 | Legacy NDC | 20241212_ff1ddeb2-9129-4c02-9757-964662dcd0ad.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7076-61 | 00904707661 | 100 BLISTER PACK in 1 CARTON (0904-7076-61) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK | 100 blister pack | 2011-06-01 | 0000-00-00 | No | No | Current |