metformin er 750 mg

Generic: metformin er 750 mg

Labeler: granules india ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin er 750 mg
Generic Name metformin er 750 mg
Labeler granules india ltd
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metformin hydrochloride 750 mg/1

Manufacturer
Granules India Ltd

Identifiers & Regulatory

Product NDC 62207-492
Product ID 62207-492_44e0f71b-ddb9-b660-e063-6294a90abf44
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209313
Listing Expiration 2026-12-31
Marketing Start 2018-06-28

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62207492
Hyphenated Format 62207-492

Supplemental Identifiers

RxCUI
860975 860981
UPC
0362207491549
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 er 750 mg (source: ndc)
Generic Name metformin er 750 mg (source: ndc)
Application Number ANDA209313 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 3500 TABLET in 1 POUCH (62207-492-40)
  • 100 TABLET in 1 BOTTLE (62207-492-43)
  • 500 TABLET in 1 BOTTLE (62207-492-47)
  • 1000 TABLET in 1 BOTTLE (62207-492-49)
  • 30 TABLET in 1 BOTTLE (62207-492-54)
source: ndc

Packages (5)

Ingredients (1)

metformin hydrochloride (750 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44e0f71b-ddb9-b660-e063-6294a90abf44", "openfda": {"upc": ["0362207491549"], "unii": ["786Z46389E"], "rxcui": ["860975", "860981"], "spl_set_id": ["b857eccf-b9ff-45ba-8241-f47f5caada2a"], "manufacturer_name": ["Granules India Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3500 TABLET in 1 POUCH (62207-492-40)", "package_ndc": "62207-492-40", "marketing_start_date": "20180628"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62207-492-43)", "package_ndc": "62207-492-43", "marketing_start_date": "20190725"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (62207-492-47)", "package_ndc": "62207-492-47", "marketing_start_date": "20190725"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62207-492-49)", "package_ndc": "62207-492-49", "marketing_start_date": "20190725"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62207-492-54)", "package_ndc": "62207-492-54", "marketing_start_date": "20190725"}], "brand_name": "Metformin ER 750 mg", "product_id": "62207-492_44e0f71b-ddb9-b660-e063-6294a90abf44", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "62207-492", "generic_name": "Metformin ER 750 mg", "labeler_name": "Granules India Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin ER 750 mg", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA209313", "marketing_category": "ANDA", "marketing_start_date": "20180628", "listing_expiration_date": "20261231"}