Duloxetine
- Product NDC
- 68001-256
- 11-digit product format
- 680010256
- Labeler code
- 68001
- Product ID
- 68001-256_c7179eef-e09a-2f0f-e053-2995a90a6309
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA090739
- Marketing category
- ANDA
- Marketing start
- 2014-03-14
- Marketing end
- 2021-11-30
- 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
- 0000-00-00
- 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 |
|---|
| 68001-256-04 | 68001025604 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-256-04) | 2014-03-14 | 0000-00-00 | No | No | Current |
| 68001-256-05 | 68001025605 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-256-05) | 2014-03-14 | 0000-00-00 | No | No | Current |
| 68001-256-08 | 68001025608 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-256-08) | 2017-01-31 | 0000-00-00 | No | No | Current |