metformin hydrochloride
Generic: metformin hydrochloride tablet
Labeler: epic pharma, llcDrug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride tablet
Labeler
epic pharma, llc
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Routes
Active Ingredients
metformin hydrochloride 1000 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42806-406
Product ID
42806-406_1edb3813-b7cb-4501-ad91-eae58624c836
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209993
Listing Expiration
2027-12-31
Marketing Start
2019-01-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42806406
Hyphenated Format
42806-406
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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 tablet (source: ndc)
Application Number
ANDA209993 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 mg/1
Packaging
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-406-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1edb3813-b7cb-4501-ad91-eae58624c836", "openfda": {"upc": ["0342806406601", "0342806405604"], "unii": ["786Z46389E"], "rxcui": ["1807894", "1807917"], "spl_set_id": ["356b02d0-d239-4441-bb33-c4c54166fcd7"], "manufacturer_name": ["EPIC PHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-406-60)", "package_ndc": "42806-406-60", "marketing_start_date": "20190104"}], "brand_name": "metformin hydrochloride", "product_id": "42806-406_1edb3813-b7cb-4501-ad91-eae58624c836", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "42806-406", "generic_name": "metformin hydrochloride tablet", "labeler_name": "EPIC PHARMA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "metformin hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA209993", "marketing_category": "ANDA", "marketing_start_date": "20190104", "listing_expiration_date": "20271231"}