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, FILM COATED
Routes
ORAL
Active Ingredients

metformin hydrochloride 850 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-143
Product ID 60687-143_23a82431-7877-94b5-e063-6394a90af9db
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203686
Listing Expiration 2026-12-31
Marketing Start 2015-09-09

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687143
Hyphenated Format 60687-143

Supplemental Identifiers

RxCUI
861004 861007 861010
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 ANDA203686 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 850 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-143-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-143-11)
source: ndc

Packages (1)

60687-143-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-143-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-143-11)

Ingredients (1)

metformin hydrochloride (850 mg/1)

Linked Drug Pages (1)

Metformin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "23a82431-7877-94b5-e063-6394a90af9db", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["dd54d30b-9390-4e5a-bf62-fbf18b91e4cd"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-143-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-143-11)", "package_ndc": "60687-143-01", "marketing_start_date": "20150909"}], "brand_name": "Metformin Hydrochloride", "product_id": "60687-143_23a82431-7877-94b5-e063-6394a90af9db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "60687-143", "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": "850 mg/1"}], "application_number": "ANDA203686", "marketing_category": "ANDA", "marketing_start_date": "20150909", "listing_expiration_date": "20261231"}