metformin hydrochloride

Generic: metformin hydrochloride tablet

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

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride tablet
Labeler granules india ltd
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metformin hydrochloride 1000 mg/1

Manufacturer
Granules India Ltd

Identifiers & Regulatory

Product NDC 62207-442
Product ID 62207-442_41464770-1d45-a647-e063-6394a90ae390
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090564
Listing Expiration 2026-12-31
Marketing Start 2019-07-04

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62207442
Hyphenated Format 62207-442

Supplemental Identifiers

RxCUI
861004 861007 861010
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 tablet (source: ndc)
Application Number ANDA090564 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (62207-442-43)
  • 500 TABLET in 1 BOTTLE (62207-442-47)
  • 1000 TABLET in 1 BOTTLE (62207-442-49)
  • 60 TABLET in 1 BOTTLE (62207-442-50)
  • 90 TABLET in 1 BOTTLE (62207-442-57)
  • 27916 TABLET in 1 DRUM (62207-442-98)
source: ndc

Packages (6)

62207-442-43 100 TABLET in 1 BOTTLE (62207-442-43) 62207-442-47 500 TABLET in 1 BOTTLE (62207-442-47) 62207-442-49 1000 TABLET in 1 BOTTLE (62207-442-49) 62207-442-50 60 TABLET in 1 BOTTLE (62207-442-50) 62207-442-57 90 TABLET in 1 BOTTLE (62207-442-57) 62207-442-98 27916 TABLET in 1 DRUM (62207-442-98)

Ingredients (1)

metformin hydrochloride (1000 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": "41464770-1d45-a647-e063-6394a90ae390", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["8cd5555c-f6b2-28d8-e053-2a95a90a5f1e"], "manufacturer_name": ["Granules India Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62207-442-43)", "package_ndc": "62207-442-43", "marketing_start_date": "20190704"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (62207-442-47)", "package_ndc": "62207-442-47", "marketing_start_date": "20190704"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62207-442-49)", "package_ndc": "62207-442-49", "marketing_start_date": "20190704"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (62207-442-50)", "package_ndc": "62207-442-50", "marketing_start_date": "20190704"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62207-442-57)", "package_ndc": "62207-442-57", "marketing_start_date": "20190704"}, {"sample": false, "description": "27916 TABLET in 1 DRUM (62207-442-98)", "package_ndc": "62207-442-98", "marketing_start_date": "20190704"}], "brand_name": "Metformin Hydrochloride", "product_id": "62207-442_41464770-1d45-a647-e063-6394a90ae390", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "62207-442", "generic_name": "Metformin Hydrochloride Tablet", "labeler_name": "Granules India Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA090564", "marketing_category": "ANDA", "marketing_start_date": "20190704", "listing_expiration_date": "20261231"}