venlafaxine hydrochloride
- Product NDC
- 70518-0742
- 11-digit product format
- 705180742
- Labeler code
- 70518
- Product ID
- 70518-0742_e220bd26-79d7-dc2f-e053-2995a90a1b75
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090174
- Marketing category
- ANDA
- Marketing start
- 2017-09-20
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 150 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 |
|---|
| 70518-0742-0 | 70518074200 | 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-0742-0) | 2017-09-20 | 0000-00-00 | No | No | Current |