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
68788-8621
Product ID
68788-8621_48f527f0-8d17-4696-acd2-e60d0056cce6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203203
Listing Expiration
2026-12-31
Marketing Start
2024-04-04
Pharmacologic Class
Established (EPC)
Mechanism of Action
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888621
Hyphenated Format
68788-8621
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
ANDA203203 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-1)
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-3)
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-6)
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-8)
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-9)
Packages (5)
68788-8621-1
14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-1)
68788-8621-3
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-3)
68788-8621-6
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-6)
68788-8621-8
120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-8)
68788-8621-9
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48f527f0-8d17-4696-acd2-e60d0056cce6", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000009724"], "unii": ["0K5C5T2QPG"], "rxcui": ["311277"], "spl_set_id": ["db42468a-450c-4b12-b2f2-e9a76e976d45"], "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 (68788-8621-1)", "package_ndc": "68788-8621-1", "marketing_start_date": "20240405"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-3)", "package_ndc": "68788-8621-3", "marketing_start_date": "20240404"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-6)", "package_ndc": "68788-8621-6", "marketing_start_date": "20240404"}, {"sample": false, "description": "120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-8)", "package_ndc": "68788-8621-8", "marketing_start_date": "20240404"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8621-9)", "package_ndc": "68788-8621-9", "marketing_start_date": "20240404"}], "brand_name": "Lansoprazole", "product_id": "68788-8621_48f527f0-8d17-4696-acd2-e60d0056cce6", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Inhibition Gastric Acid Secretion [PE]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68788-8621", "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": "ANDA203203", "marketing_category": "ANDA", "marketing_start_date": "20240404", "listing_expiration_date": "20261231"}