Metformin

Orange BookUNIISPLATC A10BA02

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeA10BA02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

ndc11
7133525241
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2524-1)
ndc11
7133525242
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2524-2)
ndc11
7133525243
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2524-3)
ndc11
7133525244
180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2524-4)
ndc11
7133525245
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2524-5)

Annotations

UNII (FDA Substance ID)

786Z46389E

METFORMIN HYDROCHLORIDE

RxCUI 235743

Orange Book

A209313

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": "71335-2524_dcd92ded-5960-4c2c-bbf9-532f8ee3b38d",
  "productndc": "71335-2524",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "209313",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "500MG",
        "product_no": "001",
        "approval_date": "Mar 16, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "750MG",
        "product_no": "002",
        "approval_date": "Mar 16, 2018"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "METFORMIN HYDROCHLORIDE",
  "proprietary_name": "Metformin",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA209313",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Metformin ER 750 mg",
  "start_marketing_date": "20180731",
  "active_numerator_strength": "750"
}

Related drugs

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