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, FILM COATED
Routes
ORAL
Active Ingredients

metformin hydrochloride 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2081
Product ID 50090-2081_65936031-8869-4d67-96ec-a13d5b19e6b7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077095
Listing Expiration 2026-12-31
Marketing Start 2005-01-14

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902081
Hyphenated Format 50090-2081

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 ANDA077095 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-2081-0)
  • 100 TABLET, FILM COATED in 1 BOTTLE (50090-2081-3)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-2081-4)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-2081-5)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-2081-6)
source: ndc

Packages (5)

50090-2081-0 60 TABLET, FILM COATED in 1 BOTTLE (50090-2081-0) 50090-2081-3 100 TABLET, FILM COATED in 1 BOTTLE (50090-2081-3) 50090-2081-4 30 TABLET, FILM COATED in 1 BOTTLE (50090-2081-4) 50090-2081-5 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-2081-5) 50090-2081-6 90 TABLET, FILM COATED in 1 BOTTLE (50090-2081-6)

Ingredients (1)

metformin hydrochloride (500 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": "65936031-8869-4d67-96ec-a13d5b19e6b7", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["23aa50c5-28fe-4322-b5c6-1f1c48409b16"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-2081-0)", "package_ndc": "50090-2081-0", "marketing_start_date": "20151008"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-2081-3)", "package_ndc": "50090-2081-3", "marketing_start_date": "20151008"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-2081-4)", "package_ndc": "50090-2081-4", "marketing_start_date": "20151008"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-2081-5)", "package_ndc": "50090-2081-5", "marketing_start_date": "20151008"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-2081-6)", "package_ndc": "50090-2081-6", "marketing_start_date": "20151008"}], "brand_name": "Metformin Hydrochloride", "product_id": "50090-2081_65936031-8869-4d67-96ec-a13d5b19e6b7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-2081", "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": "500 mg/1"}], "application_number": "ANDA077095", "marketing_category": "ANDA", "marketing_start_date": "20050114", "listing_expiration_date": "20261231"}