metformin hydrochloride

Generic: metformin hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

metformin hydrochloride 500 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1303
Product ID 71335-1303_d8117ecb-1bf3-4a68-86bd-9ddf26ac4146
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205096
Listing Expiration 2026-12-31
Marketing Start 2019-05-01

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351303
Hyphenated Format 71335-1303

Supplemental Identifiers

RxCUI
861004 861007 861010
UNII
786Z46389E

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name metformin hydrochloride (source: ndc)
Generic Name metformin hydrochloride (source: ndc)
Application Number ANDA205096 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 25 TABLET, COATED in 1 BOTTLE (71335-1303-0)
  • 30 TABLET, COATED in 1 BOTTLE (71335-1303-1)
  • 60 TABLET, COATED in 1 BOTTLE (71335-1303-2)
  • 100 TABLET, COATED in 1 BOTTLE (71335-1303-3)
  • 120 TABLET, COATED in 1 BOTTLE (71335-1303-4)
  • 90 TABLET, COATED in 1 BOTTLE (71335-1303-5)
  • 28 TABLET, COATED in 1 BOTTLE (71335-1303-6)
  • 56 TABLET, COATED in 1 BOTTLE (71335-1303-7)
  • 180 TABLET, COATED in 1 BOTTLE (71335-1303-8)
  • 10 TABLET, COATED in 1 BOTTLE (71335-1303-9)
source: ndc

Packages (10)

Ingredients (1)

metformin hydrochloride (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d8117ecb-1bf3-4a68-86bd-9ddf26ac4146", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["c2cc6c06-63bb-45f0-b318-78912abb392f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "25 TABLET, COATED in 1 BOTTLE (71335-1303-0)", "package_ndc": "71335-1303-0", "marketing_start_date": "20190821"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (71335-1303-1)", "package_ndc": "71335-1303-1", "marketing_start_date": "20190821"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (71335-1303-2)", "package_ndc": "71335-1303-2", "marketing_start_date": "20190821"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (71335-1303-3)", "package_ndc": "71335-1303-3", "marketing_start_date": "20190821"}, {"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE (71335-1303-4)", "package_ndc": "71335-1303-4", "marketing_start_date": "20190821"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71335-1303-5)", "package_ndc": "71335-1303-5", "marketing_start_date": "20190821"}, {"sample": false, "description": "28 TABLET, COATED in 1 BOTTLE (71335-1303-6)", "package_ndc": "71335-1303-6", "marketing_start_date": "20190821"}, {"sample": false, "description": "56 TABLET, COATED in 1 BOTTLE (71335-1303-7)", "package_ndc": "71335-1303-7", "marketing_start_date": "20190821"}, {"sample": false, "description": "180 TABLET, COATED in 1 BOTTLE (71335-1303-8)", "package_ndc": "71335-1303-8", "marketing_start_date": "20190821"}, {"sample": false, "description": "10 TABLET, COATED in 1 BOTTLE (71335-1303-9)", "package_ndc": "71335-1303-9", "marketing_start_date": "20190821"}], "brand_name": "Metformin Hydrochloride", "product_id": "71335-1303_d8117ecb-1bf3-4a68-86bd-9ddf26ac4146", "dosage_form": "TABLET, COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "71335-1303", "generic_name": "Metformin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA205096", "marketing_category": "ANDA", "marketing_start_date": "20190501", "listing_expiration_date": "20261231"}