metformin hydrochloride

Generic: metformin hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metformin hydrochloride 750 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0776
Product ID 71335-0776_17b869c0-6c85-4436-a3f1-2b411c2f3367
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 713350776
Hyphenated Format 71335-0776

Supplemental Identifiers

RxCUI
860975 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
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-1)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-2)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-3)
  • 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-4)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-5)
source: ndc

Packages (5)

71335-0776-1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-1) 71335-0776-2 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-2) 71335-0776-3 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-3) 71335-0776-4 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-4) 71335-0776-5 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-5)

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": "17b869c0-6c85-4436-a3f1-2b411c2f3367", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975", "860981"], "spl_set_id": ["de4a660b-172b-4c72-9e38-5634fd03cfa7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-1)", "package_ndc": "71335-0776-1", "marketing_start_date": "20180417"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-2)", "package_ndc": "71335-0776-2", "marketing_start_date": "20180417"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-3)", "package_ndc": "71335-0776-3", "marketing_start_date": "20180417"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-4)", "package_ndc": "71335-0776-4", "marketing_start_date": "20180417"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-5)", "package_ndc": "71335-0776-5", "marketing_start_date": "20180417"}], "brand_name": "Metformin Hydrochloride", "product_id": "71335-0776_17b869c0-6c85-4436-a3f1-2b411c2f3367", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "71335-0776", "generic_name": "Metformin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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"}