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United States · US · US:72603-208_c3d670fd-671b-4c32-a9ca-448dc6a49c66
arformoterol tartrate
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNorthStar RxLLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11726032083030 POUCH in 1 CARTON (72603-208-30) / 1 VIAL in 1 POUCH (72603-208-01) / 2 mL in 1 VIAL
- ndc11726032086060 POUCH in 1 CARTON (72603-208-60) / 4 VIAL in 1 POUCH (72603-208-04) / 2 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
5P8VJ2I235
ARFORMOTEROL TARTRATE
RxCUI 668284
Orange Book
A216128
AN
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "5P8VJ2I235",
"rxcui": "668284",
"inchikey": "FCSXYHUNDAXDRH-OKMNHOJOSA-N",
"display_name": "ARFORMOTEROL TARTRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "RESPIRATORY (INHALATION)",
"spl_meta": {
"f1005878-0c48-4b9a-843e-b6cf6b8bb251": {
"match": "brand_token",
"title": "ARFORMOTEROL TARTRATE SOLUTION [SUN PHARMACEUTICAL INDUSTRIES, INC.]",
"spl_version": "4",
"published_date": "2026-04-15"
}
},
"productid": "72603-208_c3d670fd-671b-4c32-a9ca-448dc6a49c66",
"productndc": "72603-208",
"dosage_form": "SOLUTION",
"orange_book": {
"appl_no": "216128",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AN",
"strength": "EQ 0.015MG BASE/2ML",
"product_no": "001",
"approval_date": "Nov 15, 2022"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ARFORMOTEROL TARTRATE",
"proprietary_name": "arformoterol tartrate",
"active_ingred_unit": "ug/2mL",
"application_number": "ANDA216128",
"marketing_category": "ANDA",
"nonproprietary_name": "arformoterol tartrate",
"start_marketing_date": "20240601",
"active_numerator_strength": "15"
}Access this data programmatically
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