lansoprazole

Generic: lansoprazole

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lansoprazole
Generic Name lansoprazole
Labeler preferred pharmaceuticals, inc.
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

lansoprazole 30 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

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)
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 687887742
Hyphenated Format 68788-7742

Supplemental Identifiers

RxCUI
311277
UNII
0K5C5T2QPG
NUI
N0000175525 N0000000147 N0000009724

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
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)
source: ndc

Packages (5)

Ingredients (1)

lansoprazole (30 mg/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"}