lansoprazole
Generic: lansoprazole
Labeler: preferred pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
lansoprazole
Generic Name
lansoprazole
Labeler
preferred pharmaceuticals, inc.
Dosage Form
CAPSULE, DELAYED RELEASE
Routes
Active Ingredients
lansoprazole 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-7742
Product ID
68788-7742_ef4a11a3-db2c-4c0b-b08c-8efb4493d5a6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205868
Listing Expiration
2026-12-31
Marketing Start
2020-07-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887742
Hyphenated Format
68788-7742
Supplemental Identifiers
RxCUI
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
lansoprazole (source: ndc)
Generic Name
lansoprazole (source: ndc)
Application Number
ANDA205868 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-1)
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-3)
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-6)
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-8)
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-9)
Packages (5)
68788-7742-1
14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-1)
68788-7742-3
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-3)
68788-7742-6
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-6)
68788-7742-8
120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-8)
68788-7742-9
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ef4a11a3-db2c-4c0b-b08c-8efb4493d5a6", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000009724"], "unii": ["0K5C5T2QPG"], "rxcui": ["311277"], "spl_set_id": ["7286d6a5-611b-4993-ab93-4899d599435d"], "pharm_class_pe": ["Inhibition Gastric Acid Secretion [PE]"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-1)", "package_ndc": "68788-7742-1", "marketing_start_date": "20200701"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-3)", "package_ndc": "68788-7742-3", "marketing_start_date": "20200701"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-6)", "package_ndc": "68788-7742-6", "marketing_start_date": "20200701"}, {"sample": false, "description": "120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-8)", "package_ndc": "68788-7742-8", "marketing_start_date": "20200701"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-9)", "package_ndc": "68788-7742-9", "marketing_start_date": "20200701"}], "brand_name": "Lansoprazole", "product_id": "68788-7742_ef4a11a3-db2c-4c0b-b08c-8efb4493d5a6", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Inhibition Gastric Acid Secretion [PE]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68788-7742", "generic_name": "Lansoprazole", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lansoprazole", "active_ingredients": [{"name": "LANSOPRAZOLE", "strength": "30 mg/1"}], "application_number": "ANDA205868", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}