Duloxetine
- Product NDC
- 55154-4981
- 11-digit product format
- 551544981
- Labeler code
- 55154
- Product ID
- 55154-4981_b097ee87-bf66-4faa-8065-239f2f04c59e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA090694
- Marketing category
- ANDA
- Marketing start
- 2013-12-23
- Marketing end
- 0000-00-00
- Substance
- DULOXETINE HYDROCHLORIDE
- Active strength
- 60 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-4981-0 | 55154498100 | 10 BLISTER PACK in 1 BAG (55154-4981-0) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK | 10 blister pack | 2013-12-23 | 0000-00-00 | No | No | Current |