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United States · US · US:60687-921_485ceb49-adae-1b29-e063-6294a90aded8
Norethindrone Acetate
Orange BookUNIISPLATC G03DC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAmerican Health Packaging
CountryUS (United States)
ATC codeG03DC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11606879212130 BLISTER PACK in 1 CARTON (60687-921-21) / 1 TABLET in 1 BLISTER PACK (60687-921-11)
Annotations
UNII (FDA Substance ID)
9S44LIC7OJ
NORETHINDRONE ACETATE
RxCUI 31983
Orange Book
A091090
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "9S44LIC7OJ",
"rxcui": "31983",
"inchikey": "IMONTRJLAWHYGT-ZCPXKWAGSA-N",
"display_name": "NORETHINDRONE ACETATE",
"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": "60687-921_485ceb49-adae-1b29-e063-6294a90aded8",
"productndc": "60687-921",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "091090",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "001",
"approval_date": "Jul 21, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NORETHINDRONE ACETATE",
"proprietary_name": "Norethindrone Acetate",
"active_ingred_unit": "mg/1",
"application_number": "ANDA091090",
"marketing_category": "ANDA",
"nonproprietary_name": "Norethindrone Acetate",
"start_marketing_date": "20260114",
"active_numerator_strength": "5"
}Related drugs
Other records sharing ATC code G03DC02.
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