VENLAFAXINE HYDROCHLORIDE
- Product NDC
- 63739-633
- 11-digit product format
- 637390633
- Labeler code
- 63739
- Product ID
- 63739-633_5e7a29ae-b697-4737-8d69-3883582e4b0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VENLAFAXINE HYDROCHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA078865
- Marketing category
- ANDA
- Marketing start
- 2011-04-14
- 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
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 |
|---|
| 63739-633-10 | 63739063310 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-633-10) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK | 10 blister pack | 2011-04-14 | 0000-00-00 | No | No | Current |