metformin hydrochloride
Generic: metformin hydrochloride
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
metformin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8564
Product ID
68788-8564_d05d2f97-e42b-43f7-a89d-820224a6822e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213320
Marketing Start
2024-01-11
Marketing End
2026-09-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888564
Hyphenated Format
68788-8564
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (68788-8564-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d05d2f97-e42b-43f7-a89d-820224a6822e", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["5073c482-952c-400c-afff-64380f133bc8"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8564-1)", "package_ndc": "68788-8564-1", "marketing_end_date": "20260930", "marketing_start_date": "20240111"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "68788-8564_d05d2f97-e42b-43f7-a89d-820224a6822e", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68788-8564", "generic_name": "metformin hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA213320", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20240111"}