Lubiprostone is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Par Pharmaceutical, Inc.. The primary component is Lubiprostone.
Product ID | 10370-266_bbbc1583-077b-44ac-a860-32221b21a291 |
NDC | 10370-266 |
Product Type | Human Prescription Drug |
Proprietary Name | Lubiprostone |
Generic Name | Lubiprostone |
Dosage Form | Capsule |
Route of Administration | ORAL |
Marketing Start Date | 2020-01-01 |
Marketing Category | ANDA / |
Application Number | ANDA201442 |
Labeler Name | Par Pharmaceutical, 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 | 2020-01-01 |
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 |