lansoprazole dr

Generic: lansoprazole dr

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lansoprazole dr
Generic Name lansoprazole dr
Labeler direct_rx
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

lansoprazole 30 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-370
Product ID 72189-370_201d8e02-32f5-a292-e063-6294a90af7bd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205868
Listing Expiration 2026-12-31
Marketing Start 2022-08-08

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 72189370
Hyphenated Format 72189-370

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 dr (source: ndc)
Generic Name lansoprazole dr (source: ndc)
Application Number ANDA205868 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-370-30)
source: ndc

Packages (1)

72189-370-30 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-370-30)

Ingredients (1)

lansoprazole (30 mg/1)

Linked Drug Pages (1)

Lansoprazole DR ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "201d8e02-32f5-a292-e063-6294a90af7bd", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000009724"], "unii": ["0K5C5T2QPG"], "rxcui": ["311277"], "spl_set_id": ["e5bcfc5b-f5a9-3260-e053-2a95a90ab70e"], "pharm_class_pe": ["Inhibition Gastric Acid Secretion [PE]"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-370-30)", "package_ndc": "72189-370-30", "marketing_start_date": "20220808"}], "brand_name": "Lansoprazole DR", "product_id": "72189-370_201d8e02-32f5-a292-e063-6294a90af7bd", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Inhibition Gastric Acid Secretion [PE]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72189-370", "generic_name": "Lansoprazole DR", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lansoprazole DR", "active_ingredients": [{"name": "LANSOPRAZOLE", "strength": "30 mg/1"}], "application_number": "ANDA205868", "marketing_category": "ANDA", "marketing_start_date": "20220808", "listing_expiration_date": "20261231"}