metformin hydrochloride
Generic: metformin hydrochloride
Labeler: redpharm drug, inc.Drug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride
Labeler
redpharm drug, inc.
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
metformin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67296-1701
Product ID
67296-1701_2c62e72c-7dec-d183-e063-6394a90a9d2b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078321
Listing Expiration
2026-12-31
Marketing Start
2019-11-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
672961701
Hyphenated Format
67296-1701
Supplemental Identifiers
RxCUI
UPC
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
ANDA078321 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-1701-6)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c62e72c-7dec-d183-e063-6394a90a9d2b", "openfda": {"upc": ["0367296170139"], "unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["fc61bafa-a506-14ae-e053-6394a90a9c7d"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-1701-6)", "package_ndc": "67296-1701-6", "marketing_start_date": "20191101"}], "brand_name": "Metformin Hydrochloride", "product_id": "67296-1701_2c62e72c-7dec-d183-e063-6394a90a9d2b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "67296-1701", "generic_name": "Metformin Hydrochloride", "labeler_name": "RedPharm Drug, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}