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 50090-6507
Product ID 50090-6507_924ca9cd-87e3-49c8-a3cf-b0275ac909d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090564
Listing Expiration 2026-12-31
Marketing Start 2019-06-26

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906507
Hyphenated Format 50090-6507

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 ANDA090564 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (50090-6507-0)
  • 100 TABLET in 1 BOTTLE (50090-6507-2)
  • 30 TABLET in 1 BOTTLE (50090-6507-3)
  • 90 TABLET in 1 BOTTLE (50090-6507-4)
  • 180 TABLET in 1 BOTTLE (50090-6507-5)
source: ndc

Packages (5)

Ingredients (1)

metformin hydrochloride (1000 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "924ca9cd-87e3-49c8-a3cf-b0275ac909d9", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["1ef6c527-89f5-4830-8900-7532b0a7ef26"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-6507-0)", "package_ndc": "50090-6507-0", "marketing_start_date": "20230531"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-6507-2)", "package_ndc": "50090-6507-2", "marketing_start_date": "20230531"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6507-3)", "package_ndc": "50090-6507-3", "marketing_start_date": "20230531"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6507-4)", "package_ndc": "50090-6507-4", "marketing_start_date": "20230531"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (50090-6507-5)", "package_ndc": "50090-6507-5", "marketing_start_date": "20230531"}], "brand_name": "Metformin Hydrochloride", "product_id": "50090-6507_924ca9cd-87e3-49c8-a3cf-b0275ac909d9", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-6507", "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": "ANDA090564", "marketing_category": "ANDA", "marketing_start_date": "20190626", "listing_expiration_date": "20261231"}