NDC 69339-162 – Lubiprostone
Lubiprostone 8 ug/1 · Capsule, Gelatin Coated · Oral
Product NDC69339-162
Product details
- Brand name
- Lubiprostone
- Generic name
- Lubiprostone
- Labeler
- Natco Pharma USA LLC
- Dosage form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA021908
- Marketed since
- October 17, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Chloride Channel Activator
Active ingredients
- Lubiprostone 8 ug/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 69339-162-17 | 40 BLISTER PACK in 1 CARTON (69339-162-17) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (69339-162-98) | Oct 17, 2022 |
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