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United States · US · US:50228-106_f1d709ff-59a3-841a-e053-2a95a90a9c29
METFORMIN HYDROCHLORIDE
Orange BookUNIISPLATC A10BA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerScieGen Pharmaceuticals Inc
CountryUS (United States)
ATC codeA10BA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc1150228106004200 TABLET in 1 BOTTLE (50228-106-00)
- ndc115022810601100 TABLET in 1 BOTTLE (50228-106-01)
- ndc115022810605500 TABLET in 1 BOTTLE (50228-106-05)
- ndc1150228106101000 TABLET in 1 BOTTLE (50228-106-10)
- ndc11502281063030 TABLET in 1 BOTTLE (50228-106-30)
Annotations
UNII (FDA Substance ID)
786Z46389E
METFORMIN HYDROCHLORIDE
RxCUI 235743
Orange Book
A203769
ABABABABAB
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": {
"1cb2b2be-595c-4e72-8d2c-c1edc7f85682": {
"match": "brand_token",
"title": "METFORMIN HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [GOLDEN STATE MEDICAL SUPPLY, INC.]",
"spl_version": "9",
"published_date": "2026-06-01"
}
},
"productid": "50228-106_f1d709ff-59a3-841a-e053-2a95a90a9c29",
"productndc": "50228-106",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "203769",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "500MG",
"product_no": "001",
"approval_date": "Sep 11, 2013"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "850MG",
"product_no": "002",
"approval_date": "Sep 11, 2013"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "1GM",
"product_no": "003",
"approval_date": "Sep 11, 2013"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "625MG",
"product_no": "004",
"approval_date": "Feb 9, 2026"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "750MG",
"product_no": "005",
"approval_date": "Feb 9, 2026"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "METFORMIN HYDROCHLORIDE",
"proprietary_name": "METFORMIN HYDROCHLORIDE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA203769",
"marketing_category": "ANDA",
"nonproprietary_name": "METFORMIN HYDROCHLORIDE",
"start_marketing_date": "20150201",
"active_numerator_strength": "850"
}Related drugs
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