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, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metformin hydrochloride 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7576
Product ID 50090-7576_50ffb93e-e184-46b1-91d1-f1cec38be49f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217631
Listing Expiration 2026-12-31
Marketing Start 2023-10-06

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907576
Hyphenated Format 50090-7576

Supplemental Identifiers

RxCUI
860975
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 ANDA217631 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-0)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-1)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-2)
  • 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-3)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-4)
source: ndc

Packages (5)

50090-7576-0 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-0) 50090-7576-1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-1) 50090-7576-2 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-2) 50090-7576-3 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-3) 50090-7576-4 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-4)

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": "50ffb93e-e184-46b1-91d1-f1cec38be49f", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["9fed67ea-7a15-4634-80cf-c975b8812ebe"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-0)", "package_ndc": "50090-7576-0", "marketing_start_date": "20250609"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-1)", "package_ndc": "50090-7576-1", "marketing_start_date": "20250609"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-2)", "package_ndc": "50090-7576-2", "marketing_start_date": "20250609"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-3)", "package_ndc": "50090-7576-3", "marketing_start_date": "20250609"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7576-4)", "package_ndc": "50090-7576-4", "marketing_start_date": "20250609"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "50090-7576_50ffb93e-e184-46b1-91d1-f1cec38be49f", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7576", "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": "ANDA217631", "marketing_category": "ANDA", "marketing_start_date": "20231006", "listing_expiration_date": "20261231"}