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United States · US · US:71335-0058_b565e019-9796-48dc-ab9e-6c939bd7c08c
Lansoprazole
Orange BookUNIISPLATC A02BC03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeA02BC03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 8
- ndc11713350058130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-1)
- ndc11713350058290 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-2)
- ndc11713350058360 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-3)
- ndc11713350058458 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-4)
- ndc11713350058528 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-5)
- ndc11713350058614 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-6)
- ndc117133500587120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-7)
- ndc117133500588180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0058-8)
Annotations
UNII (FDA Substance ID)
0K5C5T2QPG
LANSOPRAZOLE
RxCUI 17128
Orange Book
A091269
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": "71335-0058_b565e019-9796-48dc-ab9e-6c939bd7c08c",
"productndc": "71335-0058",
"dosage_form": "CAPSULE, DELAYED RELEASE",
"orange_book": {
"appl_no": "091269",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "15MG",
"product_no": "001",
"approval_date": "Oct 15, 2010"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "30MG",
"product_no": "002",
"approval_date": "Oct 15, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LANSOPRAZOLE",
"proprietary_name": "Lansoprazole",
"active_ingred_unit": "mg/1",
"application_number": "ANDA091269",
"marketing_category": "ANDA",
"nonproprietary_name": "lansoprazole",
"start_marketing_date": "20101015",
"active_numerator_strength": "15"
}Related drugs
Other records sharing ATC code A02BC03.
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