metformin hydrochloride
Generic: metformin hydrochloride
Labeler: coupler llcDrug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride
Labeler
coupler llc
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
metformin hydrochloride 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67046-1556
Product ID
67046-1556_33ec8828-24ea-8757-e063-6394a90ae222
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217631
Listing Expiration
2026-12-31
Marketing Start
2025-04-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
670461556
Hyphenated Format
67046-1556
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
ANDA217631 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1556-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "33ec8828-24ea-8757-e063-6394a90ae222", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["33ec9f6e-16d9-40ba-e063-6294a90ae87b"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1556-3)", "package_ndc": "67046-1556-3", "marketing_start_date": "20250429"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "67046-1556_33ec8828-24ea-8757-e063-6394a90ae222", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "67046-1556", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA217631", "marketing_category": "ANDA", "marketing_start_date": "20250429", "listing_expiration_date": "20261231"}