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United States · US · US:0338-0221_888f2003-1dc2-4bc0-9b3b-ebe3948b9328
Plasma-Lyte A
Orange BookUNIISPLATC C03CB
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBaxter Healthcare Corporation
CountryUS (United States)
ATC codeC03CB
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc110338022103500 mL in 1 BAG (0338-0221-03)
- ndc1103380221041000 mL in 1 BAG (0338-0221-04)
Annotations
UNII (FDA Substance ID)
02F3473H9O
MAGNESIUM CHLORIDE
RxCUI 221118
Orange Book
N017378
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "02F3473H9O",
"rxcui": "221118",
"inchikey": "DHRRIBDTHFBPNG-UHFFFAOYSA-L",
"display_name": "MAGNESIUM CHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"fe935c8d-f42d-42e4-8665-0dc66829f231": {
"match": "brand_token",
"title": "PLASMA-LYTE 148 (PH 7.4) (SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]",
"spl_version": "2",
"published_date": "2025-11-17"
}
},
"productid": "0338-0221_888f2003-1dc2-4bc0-9b3b-ebe3948b9328",
"productndc": "0338-0221",
"dosage_form": "INJECTION, SOLUTION",
"orange_book": {
"appl_no": "017378",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": true,
"rld": true,
"te_code": "AP",
"strength": "30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML",
"product_no": "002",
"approval_date": "Nov 22, 1982"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE",
"proprietary_name": "Plasma-Lyte A",
"active_ingred_unit": "mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL",
"application_number": "NDA017378",
"marketing_category": "NDA",
"nonproprietary_name": "Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride",
"start_marketing_date": "19790202",
"active_numerator_strength": "30; 37; 368; 526; 502"
}Related drugs
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