NDC 43598-168

Lubiprostone

Lubiprostone

Lubiprostone is a Oral Capsule, Gelatin Coated in the Human Prescription Drug category. It is labeled and distributed by Dr. Reddy's Laboratories Inc.. The primary component is Lubiprostone.

Product ID43598-168_ecd72df6-8058-4e44-bcc6-2c0d8d0dfef7
NDC43598-168
Product TypeHuman Prescription Drug
Proprietary NameLubiprostone
Generic NameLubiprostone
Dosage FormCapsule, Gelatin Coated
Route of AdministrationORAL
Marketing Start Date2023-01-01
Marketing CategoryNDA AUTHORIZED GENERIC /
Application NumberNDA021908
Labeler NameDr. Reddy's Laboratories Inc.
Substance NameLUBIPROSTONE
Active Ingredient Strength24 ug/1
Pharm ClassesChloride Channel Activator [EPC], Chloride Channel Activators [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 43598-168-60

60 CAPSULE, GELATIN COATED in 1 BOTTLE (43598-168-60)
Marketing Start Date2023-01-01
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Lubiprostone" or generic name "Lubiprostone"

NDCBrand NameGeneric Name
0254-3028LubiprostoneLubiprostone
0254-3029LubiprostoneLubiprostone
0480-3479LubiprostoneLubiprostone
0480-4138LubiprostoneLubiprostone
10370-266LubiprostoneLubiprostone
10370-267LubiprostoneLubiprostone
42291-475LubiprostoneLubiprostone
42291-476LubiprostoneLubiprostone
43598-163LubiprostoneLubiprostone
43598-168LubiprostoneLubiprostone
55700-963LubiprostoneLubiprostone
63304-351Lubiprostonelubiprostone
63304-352Lubiprostonelubiprostone
65162-841LubiprostoneLubiprostone
65162-842LubiprostoneLubiprostone
69339-162LUBIPROSTONELUBIPROSTONE
69339-163LUBIPROSTONELUBIPROSTONE
35356-500Amitizalubiprostone
63629-6398Amitizalubiprostone
64764-080Amitizalubiprostone
64764-240Amitizalubiprostone
68151-5003Amitizalubiprostone
72189-410AmitzaLubiprostone
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.