metformin hydrochloride
Generic: metformin hydrochloride
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
metformin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51655-556
Product ID
51655-556_494e07ae-675c-be7c-e063-6394a90a4e4a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090564
Listing Expiration
2027-12-31
Marketing Start
2022-08-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51655556
Hyphenated Format
51655-556
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 hydrochloride (source: ndc)
Generic Name
metformin hydrochloride (source: ndc)
Application Number
ANDA090564 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 60 TABLET in 1 BOTTLE, PLASTIC (51655-556-25)
- 90 TABLET in 1 BOTTLE, PLASTIC (51655-556-26)
- 30 TABLET in 1 BOTTLE, PLASTIC (51655-556-52)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "494e07ae-675c-be7c-e063-6394a90a4e4a", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["f31c08fc-cda1-349c-e053-2a95a90aba15"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (51655-556-25)", "package_ndc": "51655-556-25", "marketing_start_date": "20220916"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-556-26)", "package_ndc": "51655-556-26", "marketing_start_date": "20220811"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-556-52)", "package_ndc": "51655-556-52", "marketing_start_date": "20220916"}], "brand_name": "Metformin Hydrochloride", "product_id": "51655-556_494e07ae-675c-be7c-e063-6394a90a4e4a", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "51655-556", "generic_name": "Metformin Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA090564", "marketing_category": "ANDA", "marketing_start_date": "20220811", "listing_expiration_date": "20271231"}