metformin hcl

Generic: metformin hcl

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hcl
Generic Name metformin hcl
Labeler direct_rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metformin hydrochloride 500 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-658
Product ID 72189-658_49ee8e39-a478-065d-e063-6394a90ae127
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209882
Listing Expiration 2027-12-31
Marketing Start 2026-01-29

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189658
Hyphenated Format 72189-658

Supplemental Identifiers

RxCUI
861007
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 hcl (source: ndc)
Generic Name metformin hcl (source: ndc)
Application Number ANDA209882 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (72189-658-30)
  • 180 TABLET, FILM COATED in 1 BOTTLE (72189-658-82)
source: ndc

Packages (2)

Ingredients (1)

metformin hydrochloride (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49ee8e39-a478-065d-e063-6394a90ae127", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["498ac5fc-14be-d36a-e063-6394a90a3012"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-658-30)", "package_ndc": "72189-658-30", "marketing_start_date": "20260129"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (72189-658-82)", "package_ndc": "72189-658-82", "marketing_start_date": "20260129"}], "brand_name": "Metformin HCL", "product_id": "72189-658_49ee8e39-a478-065d-e063-6394a90ae127", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72189-658", "generic_name": "Metformin HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin HCL", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA209882", "marketing_category": "ANDA", "marketing_start_date": "20260129", "listing_expiration_date": "20271231"}