metformin hydrochloride

Generic: metformin hydrochloride

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler zydus lifesciences limited
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metformin hydrochloride 750 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 65841-039
Product ID 65841-039_d6499cd6-fa2b-4c97-8f96-37ac878f0bac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077078
Listing Expiration 2026-12-31
Marketing Start 2005-09-28

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65841039
Hyphenated Format 65841-039

Supplemental Identifiers

RxCUI
860975 860981
UNII
786Z46389E

Packaging Origin

Original Packager
true

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 ANDA077078 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-039-01)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-039-05)
source: ndc

Packages (2)

65841-039-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-039-01) 65841-039-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-039-05)

Ingredients (1)

metformin hydrochloride (750 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": "d6499cd6-fa2b-4c97-8f96-37ac878f0bac", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975", "860981"], "spl_set_id": ["a8a10ea0-7aa6-48ab-aad4-af8895636672"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-039-01)", "package_ndc": "65841-039-01", "marketing_start_date": "20050928"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-039-05)", "package_ndc": "65841-039-05", "marketing_start_date": "20050928"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "65841-039_d6499cd6-fa2b-4c97-8f96-37ac878f0bac", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "65841-039", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA077078", "marketing_category": "ANDA", "marketing_start_date": "20050928", "listing_expiration_date": "20261231"}