metformin
Generic: metformin er 500 mg
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
metformin
Generic Name
metformin er 500 mg
Labeler
remedyrepack inc.
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
metformin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3570
Product ID
70518-3570_2749b522-e8e5-dae7-e063-6394a90ae724
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209313
Marketing Start
2022-11-03
Marketing End
2027-10-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183570
Hyphenated Format
70518-3570
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 (source: ndc)
Generic Name
metformin er 500 mg (source: ndc)
Application Number
ANDA209313 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3570-0)
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3570-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2749b522-e8e5-dae7-e063-6394a90ae724", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860975"], "spl_set_id": ["4c0cb4c6-100d-46fc-9b50-03945de46c86"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3570-0)", "package_ndc": "70518-3570-0", "marketing_end_date": "20260531", "marketing_start_date": "20221103"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3570-1)", "package_ndc": "70518-3570-1", "marketing_end_date": "20271031", "marketing_start_date": "20230104"}], "brand_name": "Metformin", "product_id": "70518-3570_2749b522-e8e5-dae7-e063-6394a90ae724", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "70518-3570", "generic_name": "Metformin ER 500 mg", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA209313", "marketing_category": "ANDA", "marketing_end_date": "20271031", "marketing_start_date": "20221103"}