NDC 72189-607 – Lubiprostone
Lubiprostone 24 ug/1 · Capsule, Gelatin Coated · Oral
Product NDC72189-607
Product details
- Brand name
- Lubiprostone
- Generic name
- Lubiprostone
- Labeler
- Direct Rx
- Dosage form
- Capsule, Gelatin Coated
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA021908
- Marketed since
- January 16, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Chloride Channel Activator
Active ingredients
- Lubiprostone 24 ug/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72189-607-60 | 60 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-607-60) | Jan 16, 2025 |
Other Lubiprostone products
- 80425-0355 Lubiprostone 24 ug/1 · Capsule, Gelatin Coated · Advanced Rx of Tennessee, LLC
- 80425-0354 Lubiprostone 8 ug/1 · Capsule, Gelatin Coated · Advanced Rx of Tennessee, LLC
- 60687-827 Lubiprostone 24 ug/1 · Capsule, Gelatin Coated · American Health Packaging
- 60687-816 Lubiprostone 8 ug/1 · Capsule, Gelatin Coated · American Health Packaging
- 76420-906 Lubiprostone 8 ug/1 · Capsule, Gelatin Coated · Asclemed USA, Inc.
- 76420-907 Lubiprostone 24 ug/1 · Capsule, Gelatin Coated · Asclemed USA, Inc.
- 43598-163 Lubiprostone 8 ug/1 · Capsule, Gelatin Coated · Dr. Reddy's Laboratories Inc.
- 43598-168 Lubiprostone 24 ug/1 · Capsule, Gelatin Coated · Dr. Reddy's Laboratories Inc.
- 51407-744 Lubiprostone 8 ug/1 · Capsule, Gelatin Coated · Golden State Medical Supply, Inc.
- 51407-745 Lubiprostone 24 ug/1 · Capsule, Gelatin Coated · Golden State Medical Supply, Inc.
- 69339-162 Lubiprostone 8 ug/1 · Capsule, Gelatin Coated · Natco Pharma USA LLC
- 69339-163 Lubiprostone 24 ug/1 · Capsule, Gelatin Coated · Natco Pharma USA LLC