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
50090-7866
Product ID
50090-7866_6bd0d5de-b984-451a-ba74-f8d1f47eb3ad
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209882
Listing Expiration
2027-12-31
Marketing Start
2021-05-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907866
Hyphenated Format
50090-7866
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
ANDA209882 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 mg/1
Packaging
- 90 TABLET, FILM COATED in 1 BOTTLE (50090-7866-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6bd0d5de-b984-451a-ba74-f8d1f47eb3ad", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["8c248958-6c01-455e-89f5-959facb272ed"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7866-0)", "package_ndc": "50090-7866-0", "marketing_start_date": "20260126"}], "brand_name": "Metformin Hydrochloride", "product_id": "50090-7866_6bd0d5de-b984-451a-ba74-f8d1f47eb3ad", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7866", "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": "ANDA209882", "marketing_category": "ANDA", "marketing_start_date": "20210517", "listing_expiration_date": "20271231"}