Duloxetine Hydrochloride
- Product NDC
- 55154-7878
- 11-digit product format
- 551547878
- Labeler code
- 55154
- Product ID
- 55154-7878_dda0a470-9a2e-43a4-998c-4a3ff42d4e53
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine Hydrochloride
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA202045
- Marketing category
- ANDA
- Marketing start
- 2014-06-13
- Marketing end
- 0000-00-00
- Substance
- DULOXETINE HYDROCHLORIDE
- Active strength
- 30 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-7878-0 | 55154787800 | 10 BLISTER PACK in 1 BAG (55154-7878-0) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK | 10 blister pack | 2014-06-13 | 0000-00-00 | No | No | Current |