Duloxetine
- Product NDC
- 50090-4403
- 11-digit product format
- 500904403
- Labeler code
- 50090
- Product ID
- 50090-4403_675a88fb-b31a-4387-ab06-7f08d867e239
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090739
- Marketing category
- ANDA
- Marketing start
- 2014-05-27
- Marketing end
- 0000-00-00
- Substance
- DULOXETINE HYDROCHLORIDE
- Active strength
- 20 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4403-0 | 50090440300 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-4403-0) | 2019-06-28 | 0000-00-00 | No | No | Current |