metformin hcl

Generic: metformin hcl

Labeler: qpharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hcl
Generic Name metformin hcl
Labeler qpharma, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metformin hydrochloride 1000 mg/1

Manufacturer
QPharma, Inc.

Identifiers & Regulatory

Product NDC 42708-018
Product ID 42708-018_45b422ff-1892-ceaa-e063-6394a90a00c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090564
Listing Expiration 2026-12-31
Marketing Start 2017-02-06

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42708018
Hyphenated Format 42708-018

Supplemental Identifiers

RxCUI
861004 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 ANDA090564 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (42708-018-30)
source: ndc

Packages (1)

42708-018-30 30 TABLET in 1 BOTTLE (42708-018-30)

Ingredients (1)

metformin hydrochloride (1000 mg/1)

Linked Drug Pages (1)

Metformin HCl ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45b422ff-1892-ceaa-e063-6394a90a00c9", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004", "861007"], "spl_set_id": ["06ade2e1-5981-4e3d-b7e9-7ff083eb4551"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE (42708-018-30)", "package_ndc": "42708-018-30", "marketing_start_date": "20180730"}], "brand_name": "Metformin HCl", "product_id": "42708-018_45b422ff-1892-ceaa-e063-6394a90a00c9", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "42708-018", "generic_name": "Metformin HCl", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin HCl", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA090564", "marketing_category": "ANDA", "marketing_start_date": "20170206", "listing_expiration_date": "20261231"}