NDC 46708-280 – Duloxetine Hydrochloride
Duloxetine Hydrochloride 60 mg/1 · Capsule, Delayed Release · Oral
Product NDC46708-280
Product details
- Brand name
- Duloxetine Hydrochloride
- Generic name
- Duloxetine
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202949
- Marketed since
- June 9, 2014
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 60 mg/1
Uses, dosage, side effects and warnings for Duloxetine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 46708-280-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-280-30) | Jun 9, 2014 |
| 46708-280-90 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-280-90) | Jun 9, 2014 |
| 46708-280-91 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-280-91) | Jun 9, 2014 |
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