Lubiprostone is a Oral Capsule, Gelatin Coated in the Human Prescription Drug category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is Lubiprostone.
| Product ID | 63304-351_f08037a1-cd7d-b92e-e053-2a95a90ab04d |
| NDC | 63304-351 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Lubiprostone |
| Generic Name | Lubiprostone |
| Dosage Form | Capsule, Gelatin Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2023-01-01 |
| Marketing Category | NDA AUTHORIZED GENERIC / |
| Application Number | NDA021908 |
| Labeler Name | Sun Pharmaceutical Industries, Inc. |
| Substance Name | LUBIPROSTONE |
| Active Ingredient Strength | 8 ug/1 |
| Pharm Classes | Chloride Channel Activator [EPC], Chloride Channel Activators [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
| Marketing Start Date | 2023-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0254-3028 | Lubiprostone | Lubiprostone |
| 0254-3029 | Lubiprostone | Lubiprostone |
| 0480-3479 | Lubiprostone | Lubiprostone |
| 0480-4138 | Lubiprostone | Lubiprostone |
| 10370-266 | Lubiprostone | Lubiprostone |
| 10370-267 | Lubiprostone | Lubiprostone |
| 42291-475 | Lubiprostone | Lubiprostone |
| 42291-476 | Lubiprostone | Lubiprostone |
| 43598-163 | Lubiprostone | Lubiprostone |
| 43598-168 | Lubiprostone | Lubiprostone |
| 55700-963 | Lubiprostone | Lubiprostone |
| 63304-351 | Lubiprostone | lubiprostone |
| 63304-352 | Lubiprostone | lubiprostone |
| 65162-841 | Lubiprostone | Lubiprostone |
| 65162-842 | Lubiprostone | Lubiprostone |
| 69339-162 | LUBIPROSTONE | LUBIPROSTONE |
| 69339-163 | LUBIPROSTONE | LUBIPROSTONE |
| 35356-500 | Amitiza | lubiprostone |
| 63629-6398 | Amitiza | lubiprostone |
| 64764-080 | Amitiza | lubiprostone |
| 64764-240 | Amitiza | lubiprostone |
| 68151-5003 | Amitiza | lubiprostone |
| 72189-410 | Amitza | Lubiprostone |