metformin hydrochloride

Generic: metformin hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metformin hydrochloride 850 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-409
Product ID 72789-409_48334c7e-36f3-00ff-e063-6394a90a3f42
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213320
Marketing Start 2023-01-19
Marketing End 2027-03-31

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789409
Hyphenated Format 72789-409

Supplemental Identifiers

RxCUI
861010
UPC
0372789409900
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 ANDA213320 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 850 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-409-90)
source: ndc

Packages (1)

72789-409-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-409-90)

Ingredients (1)

metformin hydrochloride (850 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": "48334c7e-36f3-00ff-e063-6394a90a3f42", "openfda": {"upc": ["0372789409900"], "unii": ["786Z46389E"], "rxcui": ["861010"], "spl_set_id": ["e3e9b582-fd15-4fe0-a210-398d9149696e"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-409-90)", "package_ndc": "72789-409-90", "marketing_end_date": "20270331", "marketing_start_date": "20240607"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "72789-409_48334c7e-36f3-00ff-e063-6394a90a3f42", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72789-409", "generic_name": "metformin hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA213320", "marketing_category": "ANDA", "marketing_end_date": "20270331", "marketing_start_date": "20230119"}