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United States · US · US:68071-5254_1d78d7d4-4388-eab7-e063-6394a90a9e7f
Tamoxifen Citrate
Orange BookUNIISPLATC L02BA01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNuCare Pharmaceuticals,Inc.
CountryUS (United States)
ATC codeL02BA01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11680715254330 TABLET in 1 BOTTLE (68071-5254-3)
Annotations
UNII (FDA Substance ID)
7FRV7310N6
TAMOXIFEN CITRATE
RxCUI 40137
Orange Book
A070929
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "7FRV7310N6",
"rxcui": "40137",
"inchikey": "FQZYTYWMLGAPFJ-OQKDUQJOSA-N",
"display_name": "TAMOXIFEN CITRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"509f8ba3-214d-aec8-e063-6294a90af498": {
"match": "brand_token",
"title": "TAMOXIFEN CITRATE TABLET, FILM COATED [NUCARE PHARMACEUTICALS, INC.]",
"spl_version": "2",
"published_date": "2026-05-04"
}
},
"productid": "68071-5254_1d78d7d4-4388-eab7-e063-6394a90a9e7f",
"productndc": "68071-5254",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "070929",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 10MG BASE",
"product_no": "001",
"approval_date": "Feb 20, 2003"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 20MG BASE",
"product_no": "002",
"approval_date": "Feb 20, 2003"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "TAMOXIFEN CITRATE",
"proprietary_name": "Tamoxifen Citrate",
"active_ingred_unit": "mg/1",
"application_number": "ANDA070929",
"marketing_category": "ANDA",
"nonproprietary_name": "Tamoxifen Citrate",
"start_marketing_date": "20110815",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code L02BA01.
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