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United States · US · US:70069-506_ea32e1b7-7c91-478e-9a8c-85f035431e19
Cupric Chloride
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSomerset Therapeutics, LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11700695062525 VIAL, PLASTIC in 1 CARTON (70069-506-25) / 10 mL in 1 VIAL, PLASTIC (70069-506-01)
Annotations
UNII (FDA Substance ID)
S2QG84156O
CUPRIC CHLORIDE
RxCUI 21833
Orange Book
A216113
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "S2QG84156O",
"rxcui": "21833",
"inchikey": "MPTQRFCYZCXJFQ-UHFFFAOYSA-L",
"display_name": "CUPRIC CHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"86bb8a4d-6896-4901-9390-c9a194b6f0cb": {
"match": "brand_token",
"title": "CUPRIC CHLORIDE INJECTION, SOLUTION [RENOVA PHARMACEUTICALS LLC]",
"spl_version": "2",
"published_date": "2026-05-11"
}
},
"productid": "70069-506_ea32e1b7-7c91-478e-9a8c-85f035431e19",
"productndc": "70069-506",
"dosage_form": "INJECTION",
"orange_book": {
"appl_no": "216113",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 0.4MG COPPER/ML",
"product_no": "001",
"approval_date": "Apr 30, 2024"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CUPRIC CHLORIDE",
"proprietary_name": "Cupric Chloride",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA216113",
"marketing_category": "ANDA",
"nonproprietary_name": "Cupric Chloride",
"start_marketing_date": "20240514",
"active_numerator_strength": ".4"
}Access this data programmatically
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