metformin hydrochloride

Generic: metformin hydrochloride extended-release tablets

Labeler: qingdao baheal pharmaceutical co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride extended-release tablets
Labeler qingdao baheal pharmaceutical co., ltd.
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

metformin hydrochloride 1000 mg/1

Manufacturer
Qingdao BAHEAL Pharmaceutical Co., Ltd.

Identifiers & Regulatory

Product NDC 70247-018
Product ID 70247-018_48514b70-3b57-8897-e063-6294a90aa52f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209993
Listing Expiration 2027-12-31
Marketing Start 2019-03-01

Pharmacologic Class

Classes
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70247018
Hyphenated Format 70247-018

Supplemental Identifiers

RxCUI
1807894 1807917
UPC
0370247019609 0370247018602
UNII
786Z46389E

Packaging Origin

Original Packager
true

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 extended-release tablets (source: ndc)
Application Number ANDA209993 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70247-018-60)
source: ndc

Packages (1)

70247-018-60 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70247-018-60)

Ingredients (1)

metformin hydrochloride (1000 mg/1)

Linked Drug Pages (1)

Metformin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48514b70-3b57-8897-e063-6294a90aa52f", "openfda": {"upc": ["0370247019609", "0370247018602"], "unii": ["786Z46389E"], "rxcui": ["1807894", "1807917"], "spl_set_id": ["7ea6e623-4073-4671-e053-2a91aa0a3ca3"], "manufacturer_name": ["Qingdao BAHEAL Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70247-018-60)", "package_ndc": "70247-018-60", "marketing_start_date": "20190301"}], "brand_name": "Metformin Hydrochloride", "product_id": "70247-018_48514b70-3b57-8897-e063-6294a90aa52f", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "70247-018", "generic_name": "Metformin Hydrochloride Extended-Release Tablets", "labeler_name": "Qingdao BAHEAL Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA209993", "marketing_category": "ANDA", "marketing_start_date": "20190301", "listing_expiration_date": "20271231"}