NDC 31722-169 – Duloxetine
Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral
Product NDC31722-169
Product details
- Brand name
- Duloxetine
- Generic name
- Duloxetine
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA204343
- Marketed since
- December 30, 2020
- 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 |
|---|---|---|
| 31722-169-01 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-169-01) | Dec 30, 2020 |
| 31722-169-10 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-169-10) | Dec 30, 2020 |
| 31722-169-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-169-30) | Dec 30, 2020 |
| 31722-169-31 | 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (31722-169-31) | Dec 30, 2020 |
| 31722-169-32 | 105 CAPSULE, DELAYED RELEASE in 1 CARTON (31722-169-32) | Dec 30, 2020 |
| 31722-169-90 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-169-90) | Jun 29, 2024 |
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