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
Routes
ORAL
Active Ingredients

metformin hydrochloride 850 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2245
Product ID 71335-2245_0845de80-4215-480f-81ed-aecaeecaf3e0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213320
Listing Expiration 2026-12-31
Marketing Start 2023-01-19

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352245
Hyphenated Format 71335-2245

Supplemental Identifiers

RxCUI
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 ANDA213320 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 850 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (71335-2245-1)
  • 30 TABLET in 1 BOTTLE (71335-2245-2)
  • 120 TABLET in 1 BOTTLE (71335-2245-3)
  • 90 TABLET in 1 BOTTLE (71335-2245-4)
  • 100 TABLET in 1 BOTTLE (71335-2245-5)
  • 180 TABLET in 1 BOTTLE (71335-2245-6)
source: ndc

Packages (6)

71335-2245-1 60 TABLET in 1 BOTTLE (71335-2245-1) 71335-2245-2 30 TABLET in 1 BOTTLE (71335-2245-2) 71335-2245-3 120 TABLET in 1 BOTTLE (71335-2245-3) 71335-2245-4 90 TABLET in 1 BOTTLE (71335-2245-4) 71335-2245-5 100 TABLET in 1 BOTTLE (71335-2245-5) 71335-2245-6 180 TABLET in 1 BOTTLE (71335-2245-6)

Ingredients (1)

metformin hydrochloride (850 mg/1)

Linked Drug Pages (1)

METFORMIN HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0845de80-4215-480f-81ed-aecaeecaf3e0", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861010"], "spl_set_id": ["1e7ab8da-4ece-499c-b0fb-34e37d991c1c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2245-1)", "package_ndc": "71335-2245-1", "marketing_start_date": "20230925"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2245-2)", "package_ndc": "71335-2245-2", "marketing_start_date": "20230925"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2245-3)", "package_ndc": "71335-2245-3", "marketing_start_date": "20230925"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2245-4)", "package_ndc": "71335-2245-4", "marketing_start_date": "20230925"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2245-5)", "package_ndc": "71335-2245-5", "marketing_start_date": "20230925"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-2245-6)", "package_ndc": "71335-2245-6", "marketing_start_date": "20230925"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "71335-2245_0845de80-4215-480f-81ed-aecaeecaf3e0", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "71335-2245", "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": "850 mg/1"}], "application_number": "ANDA213320", "marketing_category": "ANDA", "marketing_start_date": "20230119", "listing_expiration_date": "20261231"}