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United States · US · US:43063-527_4138efd9-8582-c8db-e063-6294a90adcd7

Metformin Hydrochloride

Orange BookUNIISPLATC A10BA02

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerPD-Rx Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeA10BA02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 8

  • ndc11
    4306352714
    14 TABLET in 1 BOTTLE, PLASTIC (43063-527-14)
  • ndc11
    4306352720
    20 TABLET in 1 BOTTLE, PLASTIC (43063-527-20)
  • ndc11
    4306352730
    30 TABLET in 1 BOTTLE, PLASTIC (43063-527-30)
  • ndc11
    4306352760
    60 TABLET in 1 BOTTLE, PLASTIC (43063-527-60)
  • ndc11
    4306352790
    90 TABLET in 1 BOTTLE, PLASTIC (43063-527-90)
  • ndc11
    4306352793
    180 TABLET in 1 BOTTLE, PLASTIC (43063-527-93)
  • ndc11
    4306352794
    270 TABLET in 1 BOTTLE, PLASTIC (43063-527-94)
  • ndc11
    4306352798
    120 TABLET in 1 BOTTLE, PLASTIC (43063-527-98)

Annotations

UNII (FDA Substance ID)
786Z46389E
METFORMIN HYDROCHLORIDE
RxCUI 235743
Orange Book
A077880
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": "43063-527_4138efd9-8582-c8db-e063-6294a90adcd7",
  "productndc": "43063-527",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "077880",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "500MG",
        "product_no": "001",
        "approval_date": "Jun 5, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "850MG",
        "product_no": "002",
        "approval_date": "Jun 5, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "1GM",
        "product_no": "003",
        "approval_date": "Jun 5, 2006"
      }
    ],
    "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": "ANDA077880",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Metformin Hydrochloride",
  "start_marketing_date": "20121217",
  "active_numerator_strength": "500"
}

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