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United States · US · US:63629-7552_b5b4da2d-77d7-455b-b874-0f679a5c50dc
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 · 9
- ndc11636297552130 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-7552-1)
- ndc11636297552290 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-7552-2)
- ndc11636297552318 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-7552-3)
- ndc11636297552428 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-7552-4)
- ndc11636297552556 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-7552-5)
- ndc11636297552658 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-7552-6)
- ndc11636297552760 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-7552-7)
- ndc116362975528180 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-7552-8)
- ndc116362975529120 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-7552-9)
Annotations
UNII (FDA Substance ID)
0K5C5T2QPG
LANSOPRAZOLE
RxCUI 17128
Orange Book
A202366
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": "63629-7552_b5b4da2d-77d7-455b-b874-0f679a5c50dc",
"productndc": "63629-7552",
"dosage_form": "CAPSULE, DELAYED RELEASE PELLETS",
"orange_book": {
"appl_no": "202366",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "15MG",
"product_no": "001",
"approval_date": "Aug 19, 2013"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "30MG",
"product_no": "002",
"approval_date": "Aug 19, 2013"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LANSOPRAZOLE",
"proprietary_name": "lansoprazole",
"active_ingred_unit": "mg/1",
"application_number": "ANDA202366",
"marketing_category": "ANDA",
"nonproprietary_name": "lansoprazole",
"start_marketing_date": "20130823",
"active_numerator_strength": "30"
}Related drugs
Other records sharing ATC code A02BC03.
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