Duloxetine
- Product NDC
- 68382-387
- 11-digit product format
- 683820387
- Labeler code
- 68382
- Product ID
- 68382-387_f95fe0a8-5492-4210-87a3-1881b4e98372
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA090739
- Marketing category
- ANDA
- Marketing start
- 2014-05-27
- Marketing end
- 0000-00-00
- Substance
- DULOXETINE HYDROCHLORIDE
- Active strength
- 60 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68382-387-06 | 68382038706 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-387-06) | 2014-05-27 | 0000-00-00 | No | No | Current |
| 68382-387-10 | 68382038710 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-387-10) | 2017-04-06 | 0000-00-00 | No | No | Current |
| 68382-387-16 | 68382038716 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-387-16) | 2014-05-27 | 0000-00-00 | No | No | Current |