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, COATED
Routes
ORAL
Active Ingredients

metformin hydrochloride 1000 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7454
Product ID 50090-7454_fa439403-22cd-445b-ac1d-8f628c957a21
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205096
Listing Expiration 2026-12-31
Marketing Start 2024-03-04

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907454
Hyphenated Format 50090-7454

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 ANDA205096 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 60 TABLET, COATED in 1 BOTTLE (50090-7454-0)
  • 100 TABLET, COATED in 1 BOTTLE (50090-7454-2)
  • 30 TABLET, COATED in 1 BOTTLE (50090-7454-3)
  • 90 TABLET, COATED in 1 BOTTLE (50090-7454-4)
  • 180 TABLET, COATED in 1 BOTTLE (50090-7454-5)
source: ndc

Packages (5)

50090-7454-0 60 TABLET, COATED in 1 BOTTLE (50090-7454-0) 50090-7454-2 100 TABLET, COATED in 1 BOTTLE (50090-7454-2) 50090-7454-3 30 TABLET, COATED in 1 BOTTLE (50090-7454-3) 50090-7454-4 90 TABLET, COATED in 1 BOTTLE (50090-7454-4) 50090-7454-5 180 TABLET, COATED in 1 BOTTLE (50090-7454-5)

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": "fa439403-22cd-445b-ac1d-8f628c957a21", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["2d2ebf52-3d5e-4fad-b7f7-c9280957574c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (50090-7454-0)", "package_ndc": "50090-7454-0", "marketing_start_date": "20241113"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (50090-7454-2)", "package_ndc": "50090-7454-2", "marketing_start_date": "20241113"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (50090-7454-3)", "package_ndc": "50090-7454-3", "marketing_start_date": "20241113"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-7454-4)", "package_ndc": "50090-7454-4", "marketing_start_date": "20241113"}, {"sample": false, "description": "180 TABLET, COATED in 1 BOTTLE (50090-7454-5)", "package_ndc": "50090-7454-5", "marketing_start_date": "20241113"}], "brand_name": "Metformin Hydrochloride", "product_id": "50090-7454_fa439403-22cd-445b-ac1d-8f628c957a21", "dosage_form": "TABLET, COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7454", "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": "ANDA205096", "marketing_category": "ANDA", "marketing_start_date": "20240304", "listing_expiration_date": "20261231"}