NDC 68180-294 – Duloxetine
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral
Product NDC68180-294
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090694
- Marketed since
- December 11, 2013
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68180-294-03 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-294-03) | Dec 11, 2013 |
| 68180-294-07 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-294-07) | Dec 11, 2013 |
Recalls mentioning this NDC
- D-0097-2018 Dec 6, 2017 · Class III
Failed Dissolution Specification
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