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United States · US · US:71335-2014_0344418a-5429-4835-9f2f-0a42638d51bd
Phenazopyridine Hydrochloride
UNIISPLATC G04BX06
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeG04BX06
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 9
- ndc11713352014120 TABLET in 1 BOTTLE (71335-2014-1)
- ndc11713352014212 TABLET in 1 BOTTLE (71335-2014-2)
- ndc1171335201439 TABLET in 1 BOTTLE (71335-2014-3)
- ndc11713352014410 TABLET in 1 BOTTLE (71335-2014-4)
- ndc11713352014515 TABLET in 1 BOTTLE (71335-2014-5)
- ndc117133520146100 TABLET in 1 BOTTLE (71335-2014-6)
- ndc1171335201476 TABLET in 1 BOTTLE (71335-2014-7)
- ndc11713352014821 TABLET in 1 BOTTLE (71335-2014-8)
- ndc11713352014930 TABLET in 1 BOTTLE (71335-2014-9)
Annotations
UNII (FDA Substance ID)
0EWG668W17
PHENAZOPYRIDINE HYDROCHLORIDE
RxCUI 203197
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "0EWG668W17",
"rxcui": "203197",
"inchikey": "QQBPIHBUCMDKFG-GEEYTBSJSA-N",
"display_name": "PHENAZOPYRIDINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"6eb59b69-4ad0-47b1-bd3c-1d04d0852ec5": {
"match": "brand_token",
"title": "PHENAZOPYRIDINE HYDROCHLORIDE TABLET [REMEDYREPACK INC.]",
"spl_version": "7",
"published_date": "2026-05-20"
}
},
"productid": "71335-2014_0344418a-5429-4835-9f2f-0a42638d51bd",
"productndc": "71335-2014",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PHENAZOPYRIDINE HYDROCHLORIDE",
"proprietary_name": "Phenazopyridine Hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "Phenazopyridine",
"start_marketing_date": "20110823",
"active_numerator_strength": "100"
}Related drugs
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