metformin hydrochloride

Generic: metformin hydrochloride

Labeler: puracap laboratories llc dba blu pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler puracap laboratories llc dba blu pharmaceuticals
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metformin hydrochloride 500 mg/1

Manufacturer
PuraCap Laboratories LLC dba Blu Pharmaceuticals

Identifiers & Regulatory

Product NDC 24658-790
Product ID 24658-790_7ea9ad08-6f32-ebc1-e053-2a91aa0a7ade
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075965
Listing Expiration 2026-12-31
Marketing Start 2016-04-01

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24658790
Hyphenated Format 24658-790

Supplemental Identifiers

RxCUI
861004 861007 861010
UPC
0324658792057 0324658790015 0324658791050
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 ANDA075965 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (24658-790-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (24658-790-10)
source: ndc

Packages (2)

24658-790-01 100 TABLET, FILM COATED in 1 BOTTLE (24658-790-01) 24658-790-10 1000 TABLET, FILM COATED in 1 BOTTLE (24658-790-10)

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": "7ea9ad08-6f32-ebc1-e053-2a91aa0a7ade", "openfda": {"upc": ["0324658792057", "0324658790015", "0324658791050"], "unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["5c2581e3-2b30-4da5-8bed-228173ca20d2"], "manufacturer_name": ["PuraCap Laboratories LLC dba Blu Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (24658-790-01)", "package_ndc": "24658-790-01", "marketing_start_date": "20160401"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (24658-790-10)", "package_ndc": "24658-790-10", "marketing_start_date": "20160401"}], "brand_name": "Metformin Hydrochloride", "product_id": "24658-790_7ea9ad08-6f32-ebc1-e053-2a91aa0a7ade", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "24658-790", "generic_name": "Metformin Hydrochloride", "labeler_name": "PuraCap Laboratories LLC dba Blu Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA075965", "marketing_category": "ANDA", "marketing_start_date": "20160401", "listing_expiration_date": "20261231"}