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
50090-7116
Product ID
50090-7116_135f4763-76a5-4e71-8e5f-6d57e770d0ee
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201991
Listing Expiration
2026-12-31
Marketing Start
2013-03-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907116
Hyphenated Format
50090-7116
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
ANDA201991 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7116-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "135f4763-76a5-4e71-8e5f-6d57e770d0ee", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["a434b937-2648-4509-8ce8-94a28582ec77"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7116-0)", "package_ndc": "50090-7116-0", "marketing_start_date": "20240312"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "50090-7116_135f4763-76a5-4e71-8e5f-6d57e770d0ee", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50090-7116", "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": "ANDA201991", "marketing_category": "ANDA", "marketing_start_date": "20130301", "listing_expiration_date": "20261231"}