metformin hydrochloride
Generic: metformin hydrochloride
Labeler: chartwell rx, llcDrug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride
Labeler
chartwell rx, llc
Dosage Form
TABLET
Routes
Active Ingredients
metformin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62135-680
Product ID
62135-680_0782ae1c-d904-d465-e063-6294a90a6676
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075972
Listing Expiration
2026-12-31
Marketing Start
2002-01-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62135680
Hyphenated Format
62135-680
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 (source: ndc)
Application Number
ANDA075972 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 500 TABLET in 1 BOTTLE (62135-680-05)
- 1000 TABLET in 1 BOTTLE (62135-680-10)
- 180 TABLET in 1 BOTTLE (62135-680-18)
- 60 TABLET in 1 BOTTLE (62135-680-60)
- 90 TABLET in 1 BOTTLE (62135-680-90)
Packages (5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0782ae1c-d904-d465-e063-6294a90a6676", "openfda": {"upc": ["0362135684051", "0362135681302", "0362135682309", "0362135680053", "0362135684907", "0362135683184", "0362135680183", "0362135680909", "0362135683306", "0362135684181", "0362135683900"], "unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010", "861021", "2703582"], "spl_set_id": ["4d3dbf6f-1c8a-4daa-8343-8cd8f64a65cd"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (62135-680-05)", "package_ndc": "62135-680-05", "marketing_start_date": "20220406"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62135-680-10)", "package_ndc": "62135-680-10", "marketing_start_date": "20220406"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (62135-680-18)", "package_ndc": "62135-680-18", "marketing_start_date": "20220406"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (62135-680-60)", "package_ndc": "62135-680-60", "marketing_start_date": "20220406"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-680-90)", "package_ndc": "62135-680-90", "marketing_start_date": "20220406"}], "brand_name": "Metformin Hydrochloride", "product_id": "62135-680_0782ae1c-d904-d465-e063-6294a90a6676", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "62135-680", "generic_name": "Metformin Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA075972", "marketing_category": "ANDA", "marketing_start_date": "20020124", "listing_expiration_date": "20261231"}