Duloxetine
- Product NDC
- 70771-1344
- 11-digit product format
- 707711344
- Labeler code
- 70771
- Product ID
- 70771-1344_f1dcb903-231c-46b8-b388-ba6a3272bd9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA090728
- Marketing category
- ANDA
- Marketing start
- 2014-05-27
- Marketing end
- 0000-00-00
- Substance
- DULOXETINE HYDROCHLORIDE
- Active strength
- 20 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 |
|---|
| 70771-1344-0 | 70771134400 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1344-0) | 2017-04-06 | 0000-00-00 | No | No | Current |
| 70771-1344-3 | 70771134403 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1344-3) | 2014-05-27 | 0000-00-00 | No | No | Current |
| 70771-1344-6 | 70771134406 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1344-6) | 2014-05-27 | 0000-00-00 | No | No | Current |
| 70771-1344-9 | 70771134409 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70771-1344-9) | 2014-05-27 | 0000-00-00 | No | No | Current |