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United States · US · US:31722-204_358ef102-b287-cdc7-e063-6394a90aa4a6
pantoprazole sodium
Orange BookUNIISPLATC A02BC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCamber Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeA02BC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11317222041010 VIAL, SINGLE-DOSE in 1 CARTON (31722-204-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (31722-204-31)
- ndc11317222043225 VIAL, SINGLE-DOSE in 1 CARTON (31722-204-32) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (31722-204-31)
Annotations
UNII (FDA Substance ID)
6871619Q5X
PANTOPRAZOLE SODIUM
RxCUI 236632
Orange Book
A213778
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": "31722-204_358ef102-b287-cdc7-e063-6394a90aa4a6",
"productndc": "31722-204",
"dosage_form": "INJECTION, POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "213778",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 40MG BASE/VIAL",
"product_no": "001",
"approval_date": "May 18, 2022"
}
],
"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": "ANDA213778",
"marketing_category": "ANDA",
"nonproprietary_name": "pantoprazole sodium",
"start_marketing_date": "20220518",
"active_numerator_strength": "40"
}Related drugs
Other records sharing ATC code A02BC02.
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