metformin hydrochloride

Generic: metformin hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metformin hydrochloride 1000 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7586
Product ID 50090-7586_3c65d28f-1edf-441f-a292-9f977232793f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203769
Listing Expiration 2026-12-31
Marketing Start 2015-02-01

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907586
Hyphenated Format 50090-7586

Supplemental Identifiers

RxCUI
861004
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 ANDA203769 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (50090-7586-0)
  • 100 TABLET in 1 BOTTLE (50090-7586-2)
  • 30 TABLET in 1 BOTTLE (50090-7586-3)
  • 90 TABLET in 1 BOTTLE (50090-7586-4)
  • 180 TABLET in 1 BOTTLE (50090-7586-5)
source: ndc

Packages (5)

50090-7586-0 60 TABLET in 1 BOTTLE (50090-7586-0) 50090-7586-2 100 TABLET in 1 BOTTLE (50090-7586-2) 50090-7586-3 30 TABLET in 1 BOTTLE (50090-7586-3) 50090-7586-4 90 TABLET in 1 BOTTLE (50090-7586-4) 50090-7586-5 180 TABLET in 1 BOTTLE (50090-7586-5)

Ingredients (1)

metformin hydrochloride (1000 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": "3c65d28f-1edf-441f-a292-9f977232793f", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["ec3a9070-3745-41fb-b610-8d06129d8fd9"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-7586-0)", "package_ndc": "50090-7586-0", "marketing_start_date": "20250630"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-7586-2)", "package_ndc": "50090-7586-2", "marketing_start_date": "20250630"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7586-3)", "package_ndc": "50090-7586-3", "marketing_start_date": "20250630"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7586-4)", "package_ndc": "50090-7586-4", "marketing_start_date": "20250630"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (50090-7586-5)", "package_ndc": "50090-7586-5", "marketing_start_date": "20250630"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "50090-7586_3c65d28f-1edf-441f-a292-9f977232793f", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7586", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA203769", "marketing_category": "ANDA", "marketing_start_date": "20150201", "listing_expiration_date": "20261231"}