metformin hydrochloride

Generic: metformin hydrochloride

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metformin hydrochloride 500 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-142
Product ID 62756-142_69a60382-bf12-4627-baaf-2e0ac332b443
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077336
Listing Expiration 2026-12-31
Marketing Start 2006-02-09

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62756142
Hyphenated Format 62756-142

Supplemental Identifiers

UPC
0362756142015 0362756143012
UNII
786Z46389E

Packaging Origin

Original Packager
true

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 ANDA077336 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-01)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-02)
source: ndc

Packages (2)

62756-142-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-01) 62756-142-02 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-02)

Ingredients (1)

metformin hydrochloride (500 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": "69a60382-bf12-4627-baaf-2e0ac332b443", "openfda": {"upc": ["0362756142015", "0362756143012"], "unii": ["786Z46389E"], "spl_set_id": ["41a8bb80-7b0b-476c-8134-5d161c3239c8"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-01)", "package_ndc": "62756-142-01", "marketing_start_date": "20060209"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-02)", "package_ndc": "62756-142-02", "marketing_start_date": "20060209"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "62756-142_69a60382-bf12-4627-baaf-2e0ac332b443", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "62756-142", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077336", "marketing_category": "ANDA", "marketing_start_date": "20060209", "listing_expiration_date": "20261231"}