metformin hydrochloride

Generic: metformin hydrochloride

Labeler: redpharm drug, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler redpharm drug, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metformin hydrochloride 500 mg/1

Manufacturer
RedPharm Drug, Inc.

Identifiers & Regulatory

Product NDC 67296-1701
Product ID 67296-1701_2c62e72c-7dec-d183-e063-6394a90a9d2b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078321
Listing Expiration 2026-12-31
Marketing Start 2019-11-01

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672961701
Hyphenated Format 67296-1701

Supplemental Identifiers

RxCUI
860975
UPC
0367296170139
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 ANDA078321 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-1701-6)
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": "2c62e72c-7dec-d183-e063-6394a90a9d2b", "openfda": {"upc": ["0367296170139"], "unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["fc61bafa-a506-14ae-e053-6394a90a9c7d"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-1701-6)", "package_ndc": "67296-1701-6", "marketing_start_date": "20191101"}], "brand_name": "Metformin Hydrochloride", "product_id": "67296-1701_2c62e72c-7dec-d183-e063-6394a90a9d2b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "67296-1701", "generic_name": "Metformin Hydrochloride", "labeler_name": "RedPharm Drug, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}