NDC 33342-162 – Duloxetine Hydrochloride
Duloxetine Hydrochloride 60 mg/1 · Capsule, Delayed Release · Oral
Product NDC33342-162
Product details
- Brand name
- Duloxetine Hydrochloride
- Generic name
- Duloxetine Hydrochloride
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA204815
- Marketed since
- March 24, 2017
- Listing expires
- December 31, 2026
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 33342-162-07 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-162-07) | Mar 24, 2017 |
| 33342-162-10 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-162-10) | Mar 24, 2017 |
| 33342-162-12 | 10 BLISTER PACK in 1 CARTON (33342-162-12) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK | Mar 24, 2017 |
| 33342-162-44 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-162-44) | Mar 24, 2017 |
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