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United States · US · US:71335-2568_b59e65e1-5676-4535-920b-88b8becefc10
METFORMIN HYDROCHLORIDE
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
- ndc11713352568160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-1)
- ndc11713352568230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-2)
- ndc117133525683100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-3)
- ndc11713352568490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-4)
- ndc117133525685120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-5)
- ndc11713352568615 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-6)
- ndc11713352568745 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-7)
- ndc117133525688180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-8)
- ndc11713352568920 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-9)
Annotations
UNII (FDA Substance ID)
786Z46389E
METFORMIN HYDROCHLORIDE
RxCUI 235743
Orange Book
A217631
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": "71335-2568_b59e65e1-5676-4535-920b-88b8becefc10",
"productndc": "71335-2568",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "217631",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB1",
"strength": "500MG",
"product_no": "001",
"approval_date": "Oct 5, 2023"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "750MG",
"product_no": "002",
"approval_date": "Oct 5, 2023"
}
],
"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": "ANDA217631",
"marketing_category": "ANDA",
"nonproprietary_name": "METFORMIN HYDROCHLORIDE",
"start_marketing_date": "20231006",
"active_numerator_strength": "500"
}Related drugs
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Access this data programmatically
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