Duloxetine
- Product NDC
- 50090-2226
- 11-digit product format
- 500902226
- Labeler code
- 50090
- Product ID
- 50090-2226_6a749dc8-ec94-423e-ab7e-405995c5a306
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DULOXETINE HYDROCHLORIDE
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203088
- Marketing category
- ANDA
- Marketing start
- 2014-06-11
- Marketing end
- 0000-00-00
- Substance
- DULOXETINE HYDROCHLORIDE
- Active strength
- 60 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2226 | DULOXETINE DELAYED-RELEASE (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE PELLETS [A-S MEDICATION SOLUTIONS] | 23 | Legacy NDC | 20231211_6724528f-4542-4fac-aa76-27105444c1fd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2226-0 | 50090222600 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-2226-0) | 2015-11-09 | 0000-00-00 | No | No | Current |
| 50090-2226-1 | 50090222601 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-2226-1) | 2015-11-09 | 0000-00-00 | No | No | Current |