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United States · US · US:71335-0293_1210ee1b-4a39-4f60-af08-02eeca33dfca
METFORMIN HYDROCHLORIDE EXTENDED RELEASE
Orange BookUNIISPLATC A10BA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeA10BA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 9
- ndc11713350293160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-1)
- ndc11713350293230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-2)
- ndc117133502933100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-3)
- ndc11713350293490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-4)
- ndc117133502935120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-5)
- ndc11713350293615 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-6)
- ndc11713350293745 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-7)
- ndc117133502938180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-8)
- ndc11713350293920 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-9)
Annotations
UNII (FDA Substance ID)
786Z46389E
METFORMIN HYDROCHLORIDE
RxCUI 235743
Orange Book
A090295
AB1AB
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": "71335-0293_1210ee1b-4a39-4f60-af08-02eeca33dfca",
"productndc": "71335-0293",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "090295",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB1",
"strength": "500MG",
"product_no": "001",
"approval_date": "Apr 29, 2016"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "750MG",
"product_no": "002",
"approval_date": "Apr 29, 2016"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "METFORMIN HYDROCHLORIDE",
"proprietary_name": "METFORMIN HYDROCHLORIDE EXTENDED RELEASE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA090295",
"marketing_category": "ANDA",
"nonproprietary_name": "METFORMIN HYDROCHLORIDE",
"start_marketing_date": "20160512",
"active_numerator_strength": "500"
}Related drugs
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