metformin

Generic: metformin er 750 mg

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

Drug Facts

Product Profile

Brand Name metformin
Generic Name metformin er 750 mg
Labeler a-s medication solutions
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metformin hydrochloride 750 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7372
Product ID 50090-7372_dea33fd2-8193-4065-810a-48ec5f7a28be
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209313
Listing Expiration 2026-12-31
Marketing Start 2018-07-31

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907372
Hyphenated Format 50090-7372

Supplemental Identifiers

RxCUI
860981
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 (source: ndc)
Generic Name metformin er 750 mg (source: ndc)
Application Number ANDA209313 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7372-0)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7372-1)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7372-2)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7372-3)
source: ndc

Packages (4)

50090-7372-0 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7372-0) 50090-7372-1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7372-1) 50090-7372-2 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7372-2) 50090-7372-3 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7372-3)

Ingredients (1)

metformin hydrochloride (750 mg/1)

Linked Drug Pages (1)

Metformin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dea33fd2-8193-4065-810a-48ec5f7a28be", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["953404a4-0f03-42f1-8136-43238dad11f4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7372-0)", "package_ndc": "50090-7372-0", "marketing_start_date": "20241018"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7372-1)", "package_ndc": "50090-7372-1", "marketing_start_date": "20241018"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7372-2)", "package_ndc": "50090-7372-2", "marketing_start_date": "20241018"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7372-3)", "package_ndc": "50090-7372-3", "marketing_start_date": "20241018"}], "brand_name": "Metformin", "product_id": "50090-7372_dea33fd2-8193-4065-810a-48ec5f7a28be", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7372", "generic_name": "Metformin ER 750 mg", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA209313", "marketing_category": "ANDA", "marketing_start_date": "20180731", "listing_expiration_date": "20261231"}