Venlafaxine Hydrochloride
- Product NDC
- 55700-887
- 11-digit product format
- 557000887
- Labeler code
- 55700
- Product ID
- 55700-887_8b6f245c-c787-4f60-a7fd-345b997bbd70
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA200834
- Marketing category
- ANDA
- Marketing start
- 2020-10-28
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-887-30 | 55700088730 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55700-887-30) | 2020-10-28 | 0000-00-00 | No | No | Current |
| 55700-887-90 | 55700088790 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55700-887-90) | 2021-04-30 | 0000-00-00 | No | No | Current |