amitza
Generic: lubiprostone
Labeler: direct_rxDrug Facts
Product Profile
Brand Name
amitza
Generic Name
lubiprostone
Labeler
direct_rx
Dosage Form
CAPSULE, GELATIN COATED
Routes
Active Ingredients
lubiprostone 8 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-410
Product ID
72189-410_2c4cfec2-fedf-e007-e063-6294a90a3cf9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209920
Listing Expiration
2026-12-31
Marketing Start
2023-01-12
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189410
Hyphenated Format
72189-410
Supplemental Identifiers
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
amitza (source: ndc)
Generic Name
lubiprostone (source: ndc)
Application Number
ANDA209920 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 8 ug/1
Packaging
- 60 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-410-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4cfec2-fedf-e007-e063-6294a90a3cf9", "openfda": {"nui": ["N0000175573", "N0000175456"], "unii": ["7662KG2R6K"], "spl_set_id": ["f2121338-9586-161d-e053-2995a90af908"], "pharm_class_epc": ["Chloride Channel Activator [EPC]"], "pharm_class_moa": ["Chloride Channel Activators [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-410-60)", "package_ndc": "72189-410-60", "marketing_start_date": "20230112"}], "brand_name": "Amitza", "product_id": "72189-410_2c4cfec2-fedf-e007-e063-6294a90a3cf9", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Chloride Channel Activator [EPC]", "Chloride Channel Activators [MoA]"], "product_ndc": "72189-410", "generic_name": "Lubiprostone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitza", "active_ingredients": [{"name": "LUBIPROSTONE", "strength": "8 ug/1"}], "application_number": "ANDA209920", "marketing_category": "ANDA", "marketing_start_date": "20230112", "listing_expiration_date": "20261231"}