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 | 63304-352_f08037a1-cd7d-b92e-e053-2a95a90ab04d |
NDC | 63304-352 |
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 | 24 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 |