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United States · US · US:0008-0844_b1adaee5-9353-48ce-bde4-f169a3787e30
Protonix
Orange BookUNIISPLATC A02BC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
CountryUS (United States)
ATC codeA02BC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11000808440230 PACKET in 1 CARTON (0008-0844-02) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (0008-0844-01)
Annotations
UNII (FDA Substance ID)
6871619Q5X
PANTOPRAZOLE SODIUM
RxCUI 236632
Orange Book
N022020
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": {
"08098cb2-c048-4640-f387-6beec4a38936": {
"match": "brand_token",
"title": "PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS LLC, A SUBSIDIARY OF PFIZER INC.]",
"spl_version": "48",
"published_date": "2026-05-20"
}
},
"productid": "0008-0844_b1adaee5-9353-48ce-bde4-f169a3787e30",
"productndc": "0008-0844",
"dosage_form": "GRANULE, DELAYED RELEASE",
"orange_book": {
"appl_no": "022020",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "EQ 40MG BASE",
"product_no": "001",
"approval_date": "Nov 14, 2007"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PANTOPRAZOLE SODIUM",
"proprietary_name": "Protonix",
"active_ingred_unit": "mg/1",
"application_number": "NDA022020",
"marketing_category": "NDA",
"nonproprietary_name": "PANTOPRAZOLE SODIUM",
"start_marketing_date": "20080229",
"active_numerator_strength": "40"
}Related drugs
Other records sharing ATC code A02BC02.
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