metformin hydrochloride

Generic: metformin hydrochloride

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler northwind health company, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metformin hydrochloride 1000 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-649
Product ID 51655-649_494f8087-f75c-8014-e063-6294a90ac94c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077095
Listing Expiration 2027-12-31
Marketing Start 2021-04-01

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655649
Hyphenated Format 51655-649

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 ANDA077095 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-26)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-52)
source: ndc

Packages (2)

51655-649-26 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-26) 51655-649-52 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-52)

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": "494f8087-f75c-8014-e063-6294a90ac94c", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["db113f46-6fac-9005-e053-2995a90a017a"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-26)", "package_ndc": "51655-649-26", "marketing_start_date": "20230623"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-52)", "package_ndc": "51655-649-52", "marketing_start_date": "20210401"}], "brand_name": "Metformin Hydrochloride", "product_id": "51655-649_494f8087-f75c-8014-e063-6294a90ac94c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "51655-649", "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": "1000 mg/1"}], "application_number": "ANDA077095", "marketing_category": "ANDA", "marketing_start_date": "20210401", "listing_expiration_date": "20271231"}