metformin hcl

Generic: metformin hcl

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

Drug Facts

Product Profile

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

metformin hydrochloride 500 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-531
Product ID 72789-531_40c15fb3-40a5-08ec-e063-6294a90aec7d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090564
Listing Expiration 2026-12-31
Marketing Start 2017-02-06

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789531
Hyphenated Format 72789-531

Supplemental Identifiers

RxCUI
861007
UPC
0372789531427
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 hcl (source: ndc)
Generic Name metformin hcl (source: ndc)
Application Number ANDA090564 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 42 TABLET in 1 BOTTLE, PLASTIC (72789-531-42)
source: ndc

Packages (1)

Ingredients (1)

metformin hydrochloride (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40c15fb3-40a5-08ec-e063-6294a90aec7d", "openfda": {"upc": ["0372789531427"], "unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["c8e50300-1838-4c51-8d9d-ebbaaf0f3991"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "42 TABLET in 1 BOTTLE, PLASTIC (72789-531-42)", "package_ndc": "72789-531-42", "marketing_start_date": "20251009"}], "brand_name": "Metformin HCl", "product_id": "72789-531_40c15fb3-40a5-08ec-e063-6294a90aec7d", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72789-531", "generic_name": "Metformin HCl", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin HCl", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA090564", "marketing_category": "ANDA", "marketing_start_date": "20170206", "listing_expiration_date": "20261231"}