Cymbalta
- Product NDC
- 70518-2099
- 11-digit product format
- 705182099
- Labeler code
- 70518
- Product ID
- 70518-2099_c610614e-c0b8-8136-e053-2995a90a2b76
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine hydrochloride
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA021427
- Marketing category
- NDA
- Marketing start
- 2019-05-22
- 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
- 2022-12-31
- 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 |
|---|
| 70518-2099-0 | 70518209900 | 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-2099-0) | 2019-05-22 | 0000-00-00 | No | No | Current |