metformin hydrochloride
Generic: metformin hydrochloride
Labeler: avpakDrug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride
Labeler
avpak
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
metformin hydrochloride 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50268-551
Product ID
50268-551_47e75091-dca6-2523-e063-6394a90a54ff
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078321
Listing Expiration
2027-12-31
Marketing Start
2022-05-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50268551
Hyphenated Format
50268-551
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
ANDA078321 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 50 BLISTER PACK in 1 BOX (50268-551-15) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-551-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e75091-dca6-2523-e063-6394a90a54ff", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["de09f7a1-1e9f-60f4-e053-2a95a90a93d8"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-551-15) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-551-11)", "package_ndc": "50268-551-15", "marketing_start_date": "20220502"}], "brand_name": "Metformin Hydrochloride", "product_id": "50268-551_47e75091-dca6-2523-e063-6394a90a54ff", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "50268-551", "generic_name": "Metformin Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20220502", "listing_expiration_date": "20271231"}