metformin hydrochloride
Generic: metformin hydrochloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
metformin hydrochloride 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-548
Product ID
72789-548_47fc43fc-5333-100d-e063-6294a90a5e1b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078321
Listing Expiration
2027-12-31
Marketing Start
2024-02-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789548
Hyphenated Format
72789-548
Supplemental Identifiers
RxCUI
UPC
UNII
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
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-548-93)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47fc43fc-5333-100d-e063-6294a90a5e1b", "openfda": {"upc": ["0372789548937"], "unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["1d0b74de-ef4c-4dd2-8019-2ddb409c60b4"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-548-93)", "package_ndc": "72789-548-93", "marketing_start_date": "20260109"}], "brand_name": "Metformin Hydrochloride", "product_id": "72789-548_47fc43fc-5333-100d-e063-6294a90a5e1b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72789-548", "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": "750 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20240215", "listing_expiration_date": "20271231"}