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United States · US · US:62332-071_db0264f6-5825-49a1-bb86-746ece155660
PANTOPRAZOLE SODIUM
Orange BookUNIISPLATC A02BC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAlembic Pharmaceuticals Inc.
CountryUS (United States)
ATC codeA02BC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1162332071011 VIAL in 1 CARTON (62332-071-01) / 10 mL in 1 VIAL
- ndc11623320711010 VIAL in 1 CARTON (62332-071-10) / 10 mL in 1 VIAL
- ndc11623320712525 VIAL in 1 CARTON (62332-071-25) / 10 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
6871619Q5X
PANTOPRAZOLE SODIUM
RxCUI 236632
Orange Book
A219230
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": "62332-071_db0264f6-5825-49a1-bb86-746ece155660",
"productndc": "62332-071",
"dosage_form": "POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "219230",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 40MG BASE/VIAL",
"product_no": "001",
"approval_date": "Mar 31, 2025"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PANTOPRAZOLE SODIUM",
"proprietary_name": "PANTOPRAZOLE SODIUM",
"active_ingred_unit": "mg/10mL",
"application_number": "ANDA219230",
"marketing_category": "ANDA",
"nonproprietary_name": "pantoprazole sodium injection",
"start_marketing_date": "20250331",
"active_numerator_strength": "40"
}Related drugs
Other records sharing ATC code A02BC02.
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