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United States · US · US:60687-767_236c62bf-3ddb-0b3e-e063-6394a90ad6c6
Pantoprazole sodium
Orange BookUNIISPLATC A02BC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAmerican Health Packaging
CountryUS (United States)
ATC codeA02BC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11606877672730 PACKET in 1 CARTON (60687-767-27) / 1 FOR SUSPENSION in 1 PACKET (60687-767-99)
Annotations
UNII (FDA Substance ID)
6871619Q5X
PANTOPRAZOLE SODIUM
RxCUI 236632
Orange Book
A217416
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "6871619Q5X",
"rxcui": "236632",
"inchikey": "VNKNFEINTHUQGZ-UHFFFAOYSA-N",
"display_name": "PANTOPRAZOLE SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"52bbab54-9f11-77bc-e063-6394a90ab449": {
"match": "brand_token",
"title": "PANTOPRAZOLE SODIUM TABLET, DELAYED RELEASE [COUPLER LLC]",
"spl_version": "1",
"published_date": "2026-05-28"
}
},
"productid": "60687-767_236c62bf-3ddb-0b3e-e063-6394a90ad6c6",
"productndc": "60687-767",
"dosage_form": "FOR SUSPENSION",
"orange_book": {
"appl_no": "217416",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 40MG BASE",
"product_no": "001",
"approval_date": "Feb 9, 2023"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PANTOPRAZOLE SODIUM",
"proprietary_name": "Pantoprazole sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA217416",
"marketing_category": "ANDA",
"nonproprietary_name": "Pantoprazole sodium",
"start_marketing_date": "20230801",
"active_numerator_strength": "40"
}Related drugs
Other records sharing ATC code A02BC02.
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