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United States · US · US:16714-973_36fd9f1d-be83-4b1f-bf3d-149b3c942af8
Phytonadione
Orange BookUNIISPLATC B02BA01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNorthstar Rx LLC.
CountryUS (United States)
ATC codeB02BA01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1116714973021 BOTTLE in 1 CARTON (16714-973-02) / 30 TABLET in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
A034SE7857
PHYTONADIONE
RxCUI 11258
Orange Book
A210189
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "A034SE7857",
"rxcui": "11258",
"inchikey": null,
"display_name": "PHYTONADIONE",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"a4b394e7-b766-824e-a8bf-f56808de76e1": {
"match": "brand_token",
"title": "PHYTONADIONE INJECTION, EMULSION [XIROMED LLC]",
"spl_version": "2",
"published_date": "2026-04-09"
}
},
"productid": "16714-973_36fd9f1d-be83-4b1f-bf3d-149b3c942af8",
"productndc": "16714-973",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "210189",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "001",
"approval_date": "Feb 20, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PHYTONADIONE",
"proprietary_name": "Phytonadione",
"active_ingred_unit": "mg/1",
"application_number": "ANDA210189",
"marketing_category": "ANDA",
"nonproprietary_name": "Phytonadione",
"start_marketing_date": "20220322",
"active_numerator_strength": "5"
}Related drugs
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