metformin hydrochloride

Generic: metformin hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler american health packaging
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metformin hydrochloride 500 mg/1

Manufacturer
American Health Packaging

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
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687640
Hyphenated Format 60687-640

Supplemental Identifiers

RxCUI
860975
UNII
786Z46389E

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-640-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-640-11)
source: ndc

Packages (1)

Ingredients (1)

metformin hydrochloride (500 mg/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"}