venlafaxine
- Product NDC
- 67046-557
- 11-digit product format
- 670460557
- Labeler code
- 67046
- Product ID
- 67046-557_d69472d8-fc29-6be1-e053-2a95a90ab480
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA090555
- Marketing category
- ANDA
- Marketing start
- 2021-01-12
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 75 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67046-557-30 | 67046055730 | 30 TABLET in 1 BLISTER PACK (67046-557-30) | 30 tablet | 2021-01-12 | 0000-00-00 | No | No | Current |