Metformin hydrochloride

Orange BookUNIISPLATC A10BA02

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

Identification

ManufacturerAvKARE

CountryUS (United States)

ATC codeA10BA02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 7

ndc11
4229182510
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-825-10)
ndc11
4229182512
120 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-825-12)
ndc11
4229182518
180 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-825-18)
ndc11
4229182530
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-825-30)
ndc11
4229182536
360 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-825-36)
ndc11
4229182560
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-825-60)
ndc11
4229182590
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-825-90)

Annotations

UNII (FDA Substance ID)

786Z46389E

METFORMIN HYDROCHLORIDE

RxCUI 235743

Orange Book

A207427

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": "42291-825_42c9e096-bccc-ad6e-e063-6294a90a4e5e",
  "productndc": "42291-825",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "207427",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "500MG",
        "product_no": "001",
        "approval_date": "Dec 13, 2016"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "750MG",
        "product_no": "002",
        "approval_date": "Dec 13, 2016"
      }
    ],
    "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": "ANDA207427",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Metformin hydrochloride",
  "start_marketing_date": "20240611",
  "active_numerator_strength": "500"
}

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