Cymbalta
- Product NDC
- 55289-036
- 11-digit product format
- 552890036
- Labeler code
- 55289
- Product ID
- 55289-036_d83efcac-4e84-775c-e053-2a95a90ae6e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine hydrochloride
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA021427
- Marketing category
- NDA
- Marketing start
- 2004-08-24
- Marketing end
- 0000-00-00
- Substance
- DULOXETINE HYDROCHLORIDE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 55289-036-21 | 55289003621 | 21 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (55289-036-21) | 2016-07-13 | 0000-00-00 | No | No | Current |
| 55289-036-30 | 55289003630 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (55289-036-30) | 2016-07-13 | 0000-00-00 | No | No | Current |