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United States · US · US:50268-182_2b48bae3-c39f-1035-e063-6394a90a2cc8
Sodium Citrate and Citric Acid
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAvPAK
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11502681821540 CUP, UNIT-DOSE in 1 CARTON (50268-182-15) / 15 mL in 1 CUP, UNIT-DOSE (50268-182-11)
Annotations
UNII (FDA Substance ID)
XF417D3PSL
ANHYDROUS CITRIC ACID
RxCUI 221946
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "XF417D3PSL",
"rxcui": "221946",
"inchikey": "KRKNYBCHXYNGOX-UHFFFAOYSA-N",
"display_name": "ANHYDROUS CITRIC ACID",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"52430b12-4d5f-d1e1-e063-6394a90abd64": {
"match": "brand_token",
"title": "SODIUM FLUORIDE RINSE LIQUID [ROCKLAND COSMETICS, INC.]",
"spl_version": "1",
"published_date": "2026-05-21"
}
},
"productid": "50268-182_2b48bae3-c39f-1035-e063-6394a90a2cc8",
"productndc": "50268-182",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ANHYDROUS CITRIC ACID; SODIUM CITRATE",
"proprietary_name": "Sodium Citrate and Citric Acid",
"active_ingred_unit": "mg/5mL; mg/5mL",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "SODIUM CITRATE and CITRIC ACID MONOHYDRATE",
"start_marketing_date": "20230613",
"active_numerator_strength": "334; 500"
}Access this data programmatically
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