metformin hydrochloride

Generic: metformin hydrochloride

Labeler: lifsa drugs, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler lifsa drugs, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metformin hydrochloride 625 mg/1

Manufacturer
Lifsa Drugs, LLC

Identifiers & Regulatory

Product NDC 72336-064
Product ID 72336-064_2cda4edb-3ee7-0035-e063-6294a90a7800
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075972
Listing Expiration 2026-12-31
Marketing Start 2002-01-24

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72336064
Hyphenated Format 72336-064

Supplemental Identifiers

RxCUI
861021 2703582
UPC
0372336064309 0372336095303
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 ANDA075972 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 625 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72336-064-30)
source: ndc

Packages (1)

72336-064-30 30 TABLET in 1 BOTTLE (72336-064-30)

Ingredients (1)

metformin hydrochloride (625 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": "2cda4edb-3ee7-0035-e063-6294a90a7800", "openfda": {"upc": ["0372336064309", "0372336095303"], "unii": ["786Z46389E"], "rxcui": ["861021", "2703582"], "spl_set_id": ["a2385bcd-0943-4411-8658-c22b50360385"], "manufacturer_name": ["Lifsa Drugs, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72336-064-30)", "package_ndc": "72336-064-30", "marketing_start_date": "20220501"}], "brand_name": "Metformin Hydrochloride", "product_id": "72336-064_2cda4edb-3ee7-0035-e063-6294a90a7800", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72336-064", "generic_name": "Metformin Hydrochloride", "labeler_name": "Lifsa Drugs, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "625 mg/1"}], "application_number": "ANDA075972", "marketing_category": "ANDA", "marketing_start_date": "20020124", "listing_expiration_date": "20261231"}