metformin hcl
Generic: metformin hcl
Labeler: direct_rxDrug Facts
Product Profile
Brand Name
metformin hcl
Generic Name
metformin hcl
Labeler
direct_rx
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
metformin hydrochloride 500 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189658
Hyphenated Format
72189-658
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (72189-658-30)
- 180 TABLET, FILM COATED in 1 BOTTLE (72189-658-82)
Packages (2)
Ingredients (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"}