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United States · US · US:71335-9693_7314235c-0007-4d48-a641-1866850b49ec
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
- ndc11713359693130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9693-1)
- ndc11713359693290 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9693-2)
- ndc11713359693360 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9693-3)
- ndc11713359693458 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9693-4)
- ndc11713359693528 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9693-5)
- ndc11713359693614 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9693-6)
- ndc117133596937120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9693-7)
- ndc117133596938180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-9693-8)
Annotations
UNII (FDA Substance ID)
0K5C5T2QPG
LANSOPRAZOLE
RxCUI 17128
Orange Book
A203083
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": "71335-9693_7314235c-0007-4d48-a641-1866850b49ec",
"productndc": "71335-9693",
"dosage_form": "CAPSULE, DELAYED RELEASE",
"orange_book": {
"appl_no": "203083",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "15MG",
"product_no": "001",
"approval_date": "May 18, 2020"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "30MG",
"product_no": "002",
"approval_date": "May 18, 2020"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LANSOPRAZOLE",
"proprietary_name": "Lansoprazole",
"active_ingred_unit": "mg/1",
"application_number": "ANDA203083",
"marketing_category": "ANDA",
"nonproprietary_name": "Lansoprazole",
"start_marketing_date": "20200518",
"active_numerator_strength": "15"
}Related drugs
Other records sharing ATC code A02BC03.
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