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United States · US · US:72189-370_201d8e02-32f5-a292-e063-6294a90af7bd
Lansoprazole DR
Orange BookUNIISPLATC A02BC03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDirect_Rx
CountryUS (United States)
ATC codeA02BC03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11721893703030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-370-30)
Annotations
UNII (FDA Substance ID)
0K5C5T2QPG
LANSOPRAZOLE
RxCUI 17128
Orange Book
A205868
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "0K5C5T2QPG",
"rxcui": "17128",
"inchikey": "MJIHNNLFOKEZEW-UHFFFAOYSA-N",
"display_name": "LANSOPRAZOLE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c9a43df0-efab-4486-860f-92afdb258c8b": {
"match": "brand_token",
"title": "LANSOPRAZOLE TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE [CARDINAL HEALTH 107, LLC]",
"spl_version": "5",
"published_date": "2026-06-01"
}
},
"productid": "72189-370_201d8e02-32f5-a292-e063-6294a90af7bd",
"productndc": "72189-370",
"dosage_form": "CAPSULE, DELAYED RELEASE",
"orange_book": {
"appl_no": "205868",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "15MG",
"product_no": "001",
"approval_date": "Aug 30, 2017"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "30MG",
"product_no": "002",
"approval_date": "Aug 30, 2017"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LANSOPRAZOLE",
"proprietary_name": "Lansoprazole DR",
"active_ingred_unit": "mg/1",
"application_number": "ANDA205868",
"marketing_category": "ANDA",
"nonproprietary_name": "Lansoprazole DR",
"start_marketing_date": "20220808",
"active_numerator_strength": "30"
}Related drugs
Other records sharing ATC code A02BC03.
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