metformin hydrochloride

Generic: metformin hydrochloride

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metformin hydrochloride 850 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-842
Product ID 23155-842_5de825b4-d3e9-474d-9f17-ceed2d4ea87c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213320
Marketing Start 2023-01-19
Marketing End 2027-03-31

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155842
Hyphenated Format 23155-842

Supplemental Identifiers

RxCUI
861004 861007 861010
UPC
0042317000076
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 ANDA213320 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 850 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-842-01)
  • 500 TABLET in 1 BOTTLE (23155-842-05)
  • 1000 TABLET in 1 BOTTLE (23155-842-10)
source: ndc

Packages (3)

23155-842-01 100 TABLET in 1 BOTTLE (23155-842-01) 23155-842-05 500 TABLET in 1 BOTTLE (23155-842-05) 23155-842-10 1000 TABLET in 1 BOTTLE (23155-842-10)

Ingredients (1)

metformin hydrochloride (850 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": "5de825b4-d3e9-474d-9f17-ceed2d4ea87c", "openfda": {"upc": ["0042317000076"], "unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["b63bfafa-db4c-4fb8-84cd-ff73a5e7d320"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-842-01)", "package_ndc": "23155-842-01", "marketing_end_date": "20270331", "marketing_start_date": "20230119"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-842-05)", "package_ndc": "23155-842-05", "marketing_end_date": "20261231", "marketing_start_date": "20230119"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-842-10)", "package_ndc": "23155-842-10", "marketing_end_date": "20261130", "marketing_start_date": "20230830"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "23155-842_5de825b4-d3e9-474d-9f17-ceed2d4ea87c", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "23155-842", "generic_name": "metformin hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA213320", "marketing_category": "ANDA", "marketing_end_date": "20270331", "marketing_start_date": "20230119"}