lansoprazole

Generic: lansoprazole

Labeler: ajanta pharma usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lansoprazole
Generic Name lansoprazole
Labeler ajanta pharma usa inc.
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

lansoprazole 15 mg/1

Manufacturer
Ajanta Pharma USA Inc.

Identifiers & Regulatory

Product NDC 27241-019
Product ID 27241-019_1e0a31f6-b245-43a0-81f4-8654c4b381d2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203957
Listing Expiration 2026-12-31
Marketing Start 2016-10-18

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 27241019
Hyphenated Format 27241-019

Supplemental Identifiers

RxCUI
311277 596843
UPC
0327241019036 0327241020032
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 ANDA203957 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-019-03)
  • 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-019-10)
source: ndc

Packages (2)

27241-019-03 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-019-03) 27241-019-10 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-019-10)

Ingredients (1)

lansoprazole (15 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": "1e0a31f6-b245-43a0-81f4-8654c4b381d2", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000009724"], "upc": ["0327241019036", "0327241020032"], "unii": ["0K5C5T2QPG"], "rxcui": ["311277", "596843"], "spl_set_id": ["6b9c60e9-b0d2-4aec-a04b-ccc7a62c822b"], "pharm_class_pe": ["Inhibition Gastric Acid Secretion [PE]"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-019-03)", "package_ndc": "27241-019-03", "marketing_start_date": "20161018"}, {"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-019-10)", "package_ndc": "27241-019-10", "marketing_start_date": "20161018"}], "brand_name": "Lansoprazole", "product_id": "27241-019_1e0a31f6-b245-43a0-81f4-8654c4b381d2", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Inhibition Gastric Acid Secretion [PE]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "27241-019", "generic_name": "Lansoprazole", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lansoprazole", "active_ingredients": [{"name": "LANSOPRAZOLE", "strength": "15 mg/1"}], "application_number": "ANDA203957", "marketing_category": "ANDA", "marketing_start_date": "20161018", "listing_expiration_date": "20261231"}