🇺🇸
United States · US · US:0006-0081_4323fb1c-54a7-4648-bfe0-28fb4cb65f50
JANUMET
Orange BookUNIISPLATC A10BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMerck Sharp & Dohme LLC
CountryUS (United States)
ATC codeA10BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1100060081142 BOTTLE in 1 CARTON (0006-0081-14) / 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0006-0081-07)
- ndc11000600813130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0006-0081-31)
- ndc11000600815490 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0006-0081-54)
- ndc1100060081821000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0006-0081-82)
Annotations
UNII (FDA Substance ID)
786Z46389E
METFORMIN HYDROCHLORIDE
RxCUI 235743
Orange Book
N202270
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "786Z46389E",
"rxcui": "235743",
"inchikey": "OETHQSJEHLVLGH-UHFFFAOYSA-N",
"display_name": "METFORMIN HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"64beb3d2-3aeb-4cd5-ba11-dacf6c9a5b50": {
"match": "brand_token",
"title": "JANUMET XR (SITAGLIPTIN AND METFORMIN HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [MERCK SHARP & DOHME LLC]",
"spl_version": "43",
"published_date": "2025-03-31"
}
},
"productid": "0006-0081_4323fb1c-54a7-4648-bfe0-28fb4cb65f50",
"productndc": "0006-0081",
"dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
"orange_book": {
"appl_no": "202270",
"products": [
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "500MG;EQ 50MG BASE",
"product_no": "001",
"approval_date": "Feb 2, 2012"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "1GM;EQ 50MG BASE",
"product_no": "002",
"approval_date": "Feb 2, 2012"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "1GM;EQ 100MG BASE",
"product_no": "003",
"approval_date": "Feb 2, 2012"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE",
"proprietary_name": "JANUMET",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "NDA202270",
"marketing_category": "NDA",
"nonproprietary_name": "sitagliptin and metformin hydrochloride",
"start_marketing_date": "20120202",
"active_numerator_strength": "1000; 100"
}Related drugs
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