NDC 0480-3479 – Lubiprostone
Lubiprostone 8 ug/1 · Capsule, Gelatin Coated · Oral
Product NDC0480-3479
Product details
- Brand name
- Lubiprostone
- Generic name
- Lubiprostone
- Labeler
- Teva Pharmaceuticals, Inc.
- Dosage form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209920
- Marketed since
- January 3, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Chloride Channel Activator
Active ingredients
- Lubiprostone 8 ug/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0480-3479-06 | 60 CAPSULE, GELATIN COATED in 1 BOTTLE (0480-3479-06) | Jan 3, 2023 |
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