NDC 76420-906 – Lubiprostone
Lubiprostone 8 ug/1 · Capsule, Gelatin Coated · Oral
Product NDC76420-906
Product details
- Brand name
- Lubiprostone
- Generic name
- Lubiprostone
- Labeler
- Asclemed USA, Inc.
- Dosage form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA021908
- Marketed since
- January 1, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Chloride Channel Activator
Active ingredients
- Lubiprostone 8 ug/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 76420-906-01 | 100 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-906-01) | Jan 28, 2025 |
| 76420-906-30 | 30 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-906-30) | Jan 28, 2025 |
| 76420-906-60 | 60 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-906-60) | Jan 28, 2025 |
| 76420-906-90 | 90 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-906-90) | Jan 28, 2025 |
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