duloxetine
- Product NDC
- 23155-655
- 11-digit product format
- 231550655
- Labeler code
- 23155
- Product ID
- 23155-655_93fec042-06a2-4dc0-aa07-8cbe54e120eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- duloxetine
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc.
- Application
- ANDA202336
- Marketing category
- ANDA
- Marketing start
- 2018-06-22
- 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
- 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 |
|---|
| 23155-655-03 | 23155065503 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (23155-655-03) | 2018-06-22 | 0000-00-00 | No | No | Current |
| 23155-655-09 | 23155065509 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (23155-655-09) | 2018-06-22 | 0000-00-00 | No | No | Current |
| 23155-655-10 | 23155065510 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (23155-655-10) | 2018-06-22 | 0000-00-00 | No | No | Current |