NDC 47335-382 – Duloxetine
Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral
Product NDC47335-382
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090745
- Marketed since
- December 11, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Duloxetine Hydrochloride 30 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 47335-382-08 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-08) | Dec 11, 2013 |
| 47335-382-18 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-18) | Dec 11, 2013 |
| 47335-382-61 | 100 BLISTER PACK in 1 CARTON (47335-382-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK | Dec 11, 2013 |
| 47335-382-81 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-81) | Dec 11, 2013 |
| 47335-382-83 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-83) | Dec 11, 2013 |
| 47335-382-88 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-382-88) | Dec 11, 2013 |
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