metformin hydrochloride

Generic: metformin hydrochloride

Labeler: viona pharmaceuticals inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler viona pharmaceuticals inc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metformin hydrochloride 750 mg/1

Manufacturer
Viona Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 72578-036
Product ID 72578-036_ca52a4c2-f8fd-4395-a307-3c1ec9c3cf7f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077078
Listing Expiration 2026-12-31
Marketing Start 2019-03-15

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72578036
Hyphenated Format 72578-036

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 (72578-036-01)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-036-05)
source: ndc

Packages (2)

72578-036-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-036-01) 72578-036-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-036-05)

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": "ca52a4c2-f8fd-4395-a307-3c1ec9c3cf7f", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975", "860981"], "spl_set_id": ["85027e6c-d35b-49eb-a234-dd71aa77aee0"], "manufacturer_name": ["Viona Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-036-01)", "package_ndc": "72578-036-01", "marketing_start_date": "20190315"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-036-05)", "package_ndc": "72578-036-05", "marketing_start_date": "20190315"}], "brand_name": "Metformin Hydrochloride", "product_id": "72578-036_ca52a4c2-f8fd-4395-a307-3c1ec9c3cf7f", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72578-036", "generic_name": "Metformin Hydrochloride", "labeler_name": "Viona Pharmaceuticals Inc", "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": "20190315", "listing_expiration_date": "20261231"}