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, FILM COATED
Routes
Active Ingredients
metformin hydrochloride 1000 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-5052
Product ID
50090-5052_c8113533-5e20-4b42-9a2a-b634f32c780c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077095
Listing Expiration
2026-12-31
Marketing Start
2005-01-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500905052
Hyphenated Format
50090-5052
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
ANDA077095 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 mg/1
Packaging
- 90 TABLET, FILM COATED in 1 BOTTLE (50090-5052-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c8113533-5e20-4b42-9a2a-b634f32c780c", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["afb183f6-a13c-4f00-82d5-9fe336173d34"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-5052-0)", "package_ndc": "50090-5052-0", "marketing_start_date": "20200519"}], "brand_name": "Metformin Hydrochloride", "product_id": "50090-5052_c8113533-5e20-4b42-9a2a-b634f32c780c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-5052", "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": "1000 mg/1"}], "application_number": "ANDA077095", "marketing_category": "ANDA", "marketing_start_date": "20050114", "listing_expiration_date": "20261231"}