metformin hydrochloride

Generic: metformin hydrochloride

Labeler: cambridge therapeutics technologies, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler cambridge therapeutics technologies, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metformin hydrochloride 850 mg/1

Manufacturer
Cambridge Therapeutics Technologies, LLC

Identifiers & Regulatory

Product NDC 70882-125
Product ID 70882-125_61b6dfd4-ea72-40f3-b4cd-0a51e8a810a6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091184
Listing Expiration 2026-12-31
Marketing Start 2011-01-31

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70882125
Hyphenated Format 70882-125

Supplemental Identifiers

RxCUI
861010
UPC
0370882125307
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 ANDA091184 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 850 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70882-125-30)
source: ndc

Packages (1)

70882-125-30 30 TABLET, FILM COATED in 1 BLISTER PACK (70882-125-30)

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": "61b6dfd4-ea72-40f3-b4cd-0a51e8a810a6", "openfda": {"upc": ["0370882125307"], "unii": ["786Z46389E"], "rxcui": ["861010"], "spl_set_id": ["9c333ae3-a4df-483b-9103-762134add15e"], "manufacturer_name": ["Cambridge Therapeutics Technologies, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70882-125-30)", "package_ndc": "70882-125-30", "marketing_start_date": "20110131"}], "brand_name": "Metformin Hydrochloride", "product_id": "70882-125_61b6dfd4-ea72-40f3-b4cd-0a51e8a810a6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "70882-125", "generic_name": "Metformin Hydrochloride", "labeler_name": "Cambridge Therapeutics Technologies, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA091184", "marketing_category": "ANDA", "marketing_start_date": "20110131", "listing_expiration_date": "20261231"}