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United States · US · US:51072-088_7406132d-3c90-4bea-8a2d-c71873601f0c
Pyrantel Pamoate
UNIISPLATC P02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerJefferson Labs
CountryUS (United States)
ATC codeP02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc115107208800946 mL in 1 BOTTLE (51072-088-00)
- ndc115107208801473 mL in 1 BOTTLE (51072-088-01)
- ndc115107208802946 mL in 1 BOTTLE (51072-088-02)
- ndc115107208803473 mL in 1 BOTTLE (51072-088-03)
- ndc115107208804237 mL in 1 BOTTLE (51072-088-04)
Annotations
UNII (FDA Substance ID)
81BK194Z5M
PYRANTEL PAMOATE
RxCUI 8985
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "81BK194Z5M",
"rxcui": "8985",
"inchikey": "AQXXZDYPVDOQEE-MXDQRGINSA-N",
"display_name": "PYRANTEL PAMOATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"e2606dc6-0dd3-40b3-a290-95054e4c4a91": {
"match": "brand_token",
"title": "PYRANTEL PAMOATE POWDER [AX PHARMACEUTICAL CORP]",
"spl_version": "6",
"published_date": "2026-01-19"
}
},
"productid": "51072-088_7406132d-3c90-4bea-8a2d-c71873601f0c",
"productndc": "51072-088",
"dosage_form": "SUSPENSION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "PYRANTEL PAMOATE",
"proprietary_name": "Pyrantel Pamoate",
"active_ingred_unit": "mg/mL",
"application_number": "M024",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Pyrantel Pamoate",
"start_marketing_date": "20151121",
"active_numerator_strength": "50"
}Related drugs
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