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 1000 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7877
Product ID 50090-7877_afbcd59d-f150-4dde-8aed-116c6e45b63e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213320
Listing Expiration 2027-12-31
Marketing Start 2025-08-25

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907877
Hyphenated Format 50090-7877

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 ANDA213320 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-7877-0)
  • 100 TABLET, FILM COATED in 1 BOTTLE (50090-7877-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-7877-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-7877-4)
  • 180 TABLET, FILM COATED in 1 BOTTLE (50090-7877-5)
source: ndc

Packages (5)

50090-7877-0 60 TABLET, FILM COATED in 1 BOTTLE (50090-7877-0) 50090-7877-2 100 TABLET, FILM COATED in 1 BOTTLE (50090-7877-2) 50090-7877-3 30 TABLET, FILM COATED in 1 BOTTLE (50090-7877-3) 50090-7877-4 90 TABLET, FILM COATED in 1 BOTTLE (50090-7877-4) 50090-7877-5 180 TABLET, FILM COATED in 1 BOTTLE (50090-7877-5)

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": "afbcd59d-f150-4dde-8aed-116c6e45b63e", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["239834b0-121a-4903-b3ee-90bb4db4753b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-7877-0)", "package_ndc": "50090-7877-0", "marketing_start_date": "20260202"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-7877-2)", "package_ndc": "50090-7877-2", "marketing_start_date": "20260202"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7877-3)", "package_ndc": "50090-7877-3", "marketing_start_date": "20260202"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7877-4)", "package_ndc": "50090-7877-4", "marketing_start_date": "20260202"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-7877-5)", "package_ndc": "50090-7877-5", "marketing_start_date": "20260202"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "50090-7877_afbcd59d-f150-4dde-8aed-116c6e45b63e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7877", "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": "ANDA213320", "marketing_category": "ANDA", "marketing_start_date": "20250825", "listing_expiration_date": "20271231"}