metformin hydrochloride
Generic: metformin hydrochloride
Labeler: zydus pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride
Labeler
zydus pharmaceuticals usa inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
metformin hydrochloride 850 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68382-759
Product ID
68382-759_cb5dfb45-8968-4a83-a807-d225b427b1cb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203686
Listing Expiration
2026-12-31
Marketing Start
2014-12-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68382759
Hyphenated Format
68382-759
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA203686 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 850 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (68382-759-01)
- 500 TABLET, FILM COATED in 1 BOTTLE (68382-759-05)
- 1000 TABLET, FILM COATED in 1 BOTTLE (68382-759-10)
- 90 TABLET, FILM COATED in 1 BOTTLE (68382-759-16)
- 100 BLISTER PACK in 1 CARTON (68382-759-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-759-30)
Packages (5)
68382-759-01
100 TABLET, FILM COATED in 1 BOTTLE (68382-759-01)
68382-759-05
500 TABLET, FILM COATED in 1 BOTTLE (68382-759-05)
68382-759-10
1000 TABLET, FILM COATED in 1 BOTTLE (68382-759-10)
68382-759-16
90 TABLET, FILM COATED in 1 BOTTLE (68382-759-16)
68382-759-77
100 BLISTER PACK in 1 CARTON (68382-759-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-759-30)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cb5dfb45-8968-4a83-a807-d225b427b1cb", "openfda": {"upc": ["0368382759016"], "unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["c82a10fa-1e8e-46b6-890a-737de3f34ee1"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68382-759-01)", "package_ndc": "68382-759-01", "marketing_start_date": "20141209"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68382-759-05)", "package_ndc": "68382-759-05", "marketing_start_date": "20141209"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68382-759-10)", "package_ndc": "68382-759-10", "marketing_start_date": "20141209"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68382-759-16)", "package_ndc": "68382-759-16", "marketing_start_date": "20141209"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (68382-759-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-759-30)", "package_ndc": "68382-759-77", "marketing_start_date": "20141209"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "68382-759_cb5dfb45-8968-4a83-a807-d225b427b1cb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68382-759", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA203686", "marketing_category": "ANDA", "marketing_start_date": "20141209", "listing_expiration_date": "20261231"}