NDC 49252-007 – Duloxetine
Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral
Product NDC49252-007
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- Inventia Healthcare Limited.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202336
- Marketed since
- December 5, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 49252-007-10 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-007-10) | Dec 5, 2015 |
| 49252-007-11 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-007-11) | Dec 5, 2015 |
| 49252-007-12 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-007-12) | Dec 5, 2015 |
| 49252-007-18 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-007-18) | Dec 5, 2015 |
| 49252-007-57 | 100 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (49252-007-57) | Dec 5, 2015 |
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