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United States · US · US:11534-180_020b7f87-0f3a-4223-a402-dea12a6c53d2
POLYETHYLENE GLYCOL 3350 NF
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSUNRISE PHARMACEUTICAL, INC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc111153418019119 g in 1 BOTTLE (11534-180-19)
- ndc111153418028238 g in 1 BOTTLE (11534-180-28)
- ndc111153418050510 g in 1 BOTTLE (11534-180-50)
Annotations
UNII (FDA Substance ID)
G2M7P15E5P
POLYETHYLENE GLYCOL 3350
RxCUI 221147
Orange Book
A206105
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "G2M7P15E5P",
"rxcui": "221147",
"inchikey": null,
"display_name": "POLYETHYLENE GLYCOL 3350",
"substance_type": "polymer",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"ddc9d2b1-87d8-44fa-bac6-0a7261f33564": {
"match": "brand_token",
"title": "POLYETHYLENE GLYCOL 3350 POWDER, FOR SOLUTION [MAJOR PHARMACEUTICALS]",
"spl_version": "11",
"published_date": "2026-05-25"
}
},
"productid": "11534-180_020b7f87-0f3a-4223-a402-dea12a6c53d2",
"productndc": "11534-180",
"dosage_form": "POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "206105",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "17GM/SCOOPFUL",
"product_no": "001",
"approval_date": "Oct 28, 2016"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "POLYETHYLENE GLYCOL 3350",
"proprietary_name": "POLYETHYLENE GLYCOL 3350 NF",
"active_ingred_unit": "g/17g",
"application_number": "ANDA206105",
"marketing_category": "ANDA",
"nonproprietary_name": "polyethylene glycol 3350",
"start_marketing_date": "20170613",
"active_numerator_strength": "17"
}Access this data programmatically
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