metformin hydrochloride
Generic: metformin hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
metformin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7577
Product ID
50090-7577_acd062d5-25ff-4e49-8605-30cbee1d0258
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217631
Listing Expiration
2026-12-31
Marketing Start
2023-10-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907577
Hyphenated Format
50090-7577
Supplemental Identifiers
RxCUI
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
ANDA217631 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7577-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "acd062d5-25ff-4e49-8605-30cbee1d0258", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["2d68fd88-c591-4577-a7c3-901338bdaf90"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7577-0)", "package_ndc": "50090-7577-0", "marketing_start_date": "20250609"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "50090-7577_acd062d5-25ff-4e49-8605-30cbee1d0258", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7577", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA217631", "marketing_category": "ANDA", "marketing_start_date": "20231006", "listing_expiration_date": "20261231"}