lansoprazole

Generic: lansoprazole

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lansoprazole
Generic Name lansoprazole
Labeler bluepoint laboratories
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

lansoprazole 30 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-112
Product ID 68001-112_e1e35404-0cf3-e40d-e053-2995a90a3829
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091269
Listing Expiration 2026-12-31
Marketing Start 2013-12-01

Pharmacologic Class

Established (EPC)
proton pump inhibitor [epc]
Mechanism of Action
proton pump inhibitors [moa]
Physiologic Effect
inhibition gastric acid secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68001112
Hyphenated Format 68001-112

Supplemental Identifiers

RxCUI
311277 596843
UPC
0368001111058 0368001112048
UNII
0K5C5T2QPG
NUI
N0000175525 N0000000147 N0000009724

Packaging Origin

Original Packager
true

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 ANDA091269 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-03)
  • 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-04)
  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-05)
source: ndc

Packages (3)

68001-112-03 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-03) 68001-112-04 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-04) 68001-112-05 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-05)

Ingredients (1)

lansoprazole (30 mg/1)

Linked Drug Pages (1)

Lansoprazole ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e1e35404-0cf3-e40d-e053-2995a90a3829", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000009724"], "upc": ["0368001111058", "0368001112048"], "unii": ["0K5C5T2QPG"], "rxcui": ["311277", "596843"], "spl_set_id": ["924c5a35-4804-4e14-a2fc-2b84d186d257"], "pharm_class_pe": ["Inhibition Gastric Acid Secretion [PE]"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-03)", "package_ndc": "68001-112-03", "marketing_start_date": "20131201"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-04)", "package_ndc": "68001-112-04", "marketing_start_date": "20200831"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-05)", "package_ndc": "68001-112-05", "marketing_start_date": "20131201"}], "brand_name": "Lansoprazole", "product_id": "68001-112_e1e35404-0cf3-e40d-e053-2995a90a3829", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Inhibition Gastric Acid Secretion [PE]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68001-112", "generic_name": "lansoprazole", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lansoprazole", "active_ingredients": [{"name": "LANSOPRAZOLE", "strength": "30 mg/1"}], "application_number": "ANDA091269", "marketing_category": "ANDA", "marketing_start_date": "20131201", "listing_expiration_date": "20261231"}