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United States · US · US:68382-824_c36f7488-a329-4113-8027-dfc92bbc6bbc
Sevelamer carbonate
Orange BookUNIISPLATC V03AE02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerZydus Pharmaceuticals USA Inc.
CountryUS (United States)
ATC codeV03AE02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1168382824101000 TABLET, FILM COATED in 1 BOTTLE (68382-824-10)
- ndc116838282427270 TABLET, FILM COATED in 1 BOTTLE (68382-824-27)
- ndc11683828247710 BLISTER PACK in 1 CARTON (68382-824-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-824-30)
Annotations
UNII (FDA Substance ID)
9YCX42I8IU
SEVELAMER CARBONATE
RxCUI 660890
Orange Book
A207759
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "9YCX42I8IU",
"rxcui": "660890",
"inchikey": null,
"display_name": "SEVELAMER CARBONATE",
"substance_type": "polymer",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"51ce2ed6-3acf-a6ea-e063-6294a90a21aa": {
"match": "brand_token",
"title": "SEVELAMER CARBONATE TABLET, FILM COATED [INSIGNAMEDEX LLC]",
"spl_version": "2",
"published_date": "2026-05-25"
}
},
"productid": "68382-824_c36f7488-a329-4113-8027-dfc92bbc6bbc",
"productndc": "68382-824",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "207759",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "800MG",
"product_no": "001",
"approval_date": "Aug 11, 2020"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SEVELAMER CARBONATE",
"proprietary_name": "Sevelamer carbonate",
"active_ingred_unit": "mg/1",
"application_number": "ANDA207759",
"marketing_category": "ANDA",
"nonproprietary_name": "Sevelamer carbonate",
"start_marketing_date": "20200917",
"active_numerator_strength": "800"
}Related drugs
Other records sharing ATC code V03AE02.
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