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United States · US · US:72572-553_9d6f752f-428f-455d-8f09-3b74c68524fb
Pantoprazole Sodium
Orange BookUNIISPLATC A02BC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCivica, Inc.
CountryUS (United States)
ATC codeA02BC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11725725531010 VIAL in 1 CARTON (72572-553-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (72572-553-01)
Annotations
UNII (FDA Substance ID)
6871619Q5X
PANTOPRAZOLE SODIUM
RxCUI 236632
Orange Book
N209463
AP
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": "INTRAVENOUS",
"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": "72572-553_9d6f752f-428f-455d-8f09-3b74c68524fb",
"productndc": "72572-553",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"orange_book": {
"appl_no": "209463",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AP",
"strength": "EQ 40MG BASE/VIAL",
"product_no": "001",
"approval_date": "Jun 30, 2017"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PANTOPRAZOLE SODIUM",
"proprietary_name": "Pantoprazole Sodium",
"active_ingred_unit": "mg/1",
"application_number": "NDA209463",
"marketing_category": "NDA",
"nonproprietary_name": "Pantoprazole Sodium",
"start_marketing_date": "20250601",
"active_numerator_strength": "40"
}Related drugs
Other records sharing ATC code A02BC02.
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