Duloxetine
- Product NDC
- 65862-451
- 11-digit product format
- 658620451
- Labeler code
- 65862
- Product ID
- 65862-451_f64ca39e-f7fc-45e5-a2bf-23b39ada6998
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine Hydrochloride
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA090778
- Marketing category
- ANDA
- Marketing start
- 2013-12-11
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65862-451-60 | 65862045160 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65862-451-60) | | 2013-12-11 | 0000-00-00 | No | No | Current |
| 65862-451-71 | 65862045171 | 7000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65862-451-71) | | 2013-12-11 | 0000-00-00 | No | No | Current |
| 65862-451-78 | 65862045178 | 10 BLISTER PACK in 1 CARTON (65862-451-78) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (65862-451-10) | 10 blister pack | 2013-12-11 | 0000-00-00 | No | No | Current |
| 65862-451-99 | 65862045199 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65862-451-99) | | 2013-12-11 | 0000-00-00 | No | No | Current |