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United States · US · US:68180-876_21d08d75-2957-4610-94c1-76c844ba2f1b
NORETHINDRONE
Orange BookUNIISPLATC G03DC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLupin Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeG03DC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1168180876733 BLISTER PACK in 1 CARTON (68180-876-73) / 28 TABLET in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
T18F433X4S
NORETHINDRONE
RxCUI 7514
Orange Book
A091325
AB1
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "T18F433X4S",
"rxcui": "7514",
"inchikey": "VIKNJXKGJWUCNN-XGXHKTLJSA-N",
"display_name": "NORETHINDRONE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"38924c83-53aa-4279-8f0e-1a5d8f5fd8ad": {
"match": "brand_token",
"title": "NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL TABLET [A-S MEDICATION SOLUTIONS]",
"spl_version": "7",
"published_date": "2026-03-27"
}
},
"productid": "68180-876_21d08d75-2957-4610-94c1-76c844ba2f1b",
"productndc": "68180-876",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "091325",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB1",
"strength": "0.35MG",
"product_no": "001",
"approval_date": "Sep 19, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NORETHINDRONE",
"proprietary_name": "NORETHINDRONE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA091325",
"marketing_category": "ANDA",
"nonproprietary_name": "NORETHINDRONE",
"start_marketing_date": "20201111",
"active_numerator_strength": ".35"
}Related drugs
Other records sharing ATC code G03DC02.
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