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United States · US · US:0555-9008_9ac007e4-792d-4122-8daf-456dea28f82f
Nortrel
Orange BookSPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTeva Pharmaceuticals USA, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1105559008673 POUCH in 1 CARTON (0555-9008-67) / 1 BLISTER PACK in 1 POUCH (0555-9008-79) / 1 KIT in 1 BLISTER PACK
Annotations
Orange Book
A072695
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"140c50d6-c931-423a-9aa0-526eae7ab93c": {
"match": "brand_token",
"title": "NORTREL 21 DAY (NORETHINDRONE AND ETHINYL ESTRADIOL) TABLET NORTREL 28 DAY (NORETHINDRONE AND ETHINYL ESTRADIOL) KIT [TEVA PHARMACEUTICALS USA, INC.]",
"spl_version": "16",
"published_date": "2026-01-28"
}
},
"productid": "0555-9008_9ac007e4-792d-4122-8daf-456dea28f82f",
"productndc": "0555-9008",
"dosage_form": "KIT",
"orange_book": {
"appl_no": "072695",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.035MG;0.5MG",
"product_no": "001",
"approval_date": "Feb 28, 1992"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": null,
"proprietary_name": "Nortrel",
"active_ingred_unit": null,
"application_number": "ANDA072695",
"marketing_category": "ANDA",
"nonproprietary_name": "Norethindrone and Ethinyl Estradiol",
"start_marketing_date": "20010606",
"active_numerator_strength": null
}Access this data programmatically
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