metformin hydrochloride

Generic: metformin hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler proficient rx lp
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metformin hydrochloride 750 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-141
Product ID 71205-141_35558fc3-36ae-4d1a-9bd0-404283383955
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078321
Listing Expiration 2026-12-31
Marketing Start 2008-04-17

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205141
Hyphenated Format 71205-141

Supplemental Identifiers

RxCUI
860981
UNII
786Z46389E

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 ANDA078321 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-00)
  • 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-20)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-60)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-90)
source: ndc

Packages (5)

71205-141-00 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-00) 71205-141-20 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-20) 71205-141-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-30) 71205-141-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-60) 71205-141-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-90)

Ingredients (1)

metformin hydrochloride (750 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": "35558fc3-36ae-4d1a-9bd0-404283383955", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["6f6118c1-cecc-4d7b-9965-7b114a1ad56b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-00)", "package_ndc": "71205-141-00", "marketing_start_date": "20181001"}, {"sample": false, "description": "20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-20)", "package_ndc": "71205-141-20", "marketing_start_date": "20181001"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-30)", "package_ndc": "71205-141-30", "marketing_start_date": "20181001"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-60)", "package_ndc": "71205-141-60", "marketing_start_date": "20181001"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-141-90)", "package_ndc": "71205-141-90", "marketing_start_date": "20181001"}], "brand_name": "Metformin Hydrochloride", "product_id": "71205-141_35558fc3-36ae-4d1a-9bd0-404283383955", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "71205-141", "generic_name": "Metformin Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20080417", "listing_expiration_date": "20261231"}