Venlafaxine Hydrochloride
- Product NDC
- 70518-0982
- 11-digit product format
- 705180982
- Labeler code
- 70518
- Product ID
- 70518-0982_a5ee64a8-4fe6-1b4f-e053-2995a90a7d78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA200834
- Marketing category
- ANDA
- Marketing start
- 2018-01-22
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0982 | VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [REMEDYREPACK INC.] | 11 | Legacy NDC | 20250504_ce62746f-1c6d-41fc-9036-b103129de9b7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0982-0 | 70518098200 | 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-0982-0) | 2018-01-22 | 0000-00-00 | No | No | Current |