metformin hydrochloride
Generic: metformin hydrochloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride
Labeler
american health packaging
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
metformin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-640
Product ID
60687-640_1b17db38-00f5-5bd4-e063-6294a90ae61b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206145
Marketing Start
2021-10-27
Marketing End
2026-03-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687640
Hyphenated Format
60687-640
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
ANDA206145 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-640-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-640-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b17db38-00f5-5bd4-e063-6294a90ae61b", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["42e9644e-299d-4033-9a73-54c183d6ccea"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-640-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-640-11)", "package_ndc": "60687-640-01", "marketing_end_date": "20260331", "marketing_start_date": "20211027"}], "brand_name": "Metformin Hydrochloride", "product_id": "60687-640_1b17db38-00f5-5bd4-e063-6294a90ae61b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "60687-640", "generic_name": "Metformin Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA206145", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20211027"}