metformin hydrochloride er
Generic: metformin hydrochloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
metformin hydrochloride er
Generic Name
metformin hydrochloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
metformin hydrochloride 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-106
Product ID
72789-106_4af6702a-f722-1549-e063-6294a90a6615
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207427
Listing Expiration
2027-12-31
Marketing Start
2018-06-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789106
Hyphenated Format
72789-106
Supplemental Identifiers
RxCUI
UPC
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 er (source: ndc)
Generic Name
metformin hydrochloride (source: ndc)
Application Number
ANDA207427 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-01)
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-82)
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-90)
- 180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-93)
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-95)
Packages (5)
72789-106-01
100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-01)
72789-106-82
500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-82)
72789-106-90
90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-90)
72789-106-93
180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-93)
72789-106-95
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-95)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4af6702a-f722-1549-e063-6294a90a6615", "openfda": {"upc": ["0372789106908", "0372789105604"], "unii": ["786Z46389E"], "rxcui": ["860975", "860981"], "spl_set_id": ["17050df5-9e95-4e1b-ac75-34add289b139"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-01)", "package_ndc": "72789-106-01", "marketing_start_date": "20200420"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-82)", "package_ndc": "72789-106-82", "marketing_start_date": "20200129"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-90)", "package_ndc": "72789-106-90", "marketing_start_date": "20200824"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-93)", "package_ndc": "72789-106-93", "marketing_start_date": "20200824"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-95)", "package_ndc": "72789-106-95", "marketing_start_date": "20200129"}], "brand_name": "Metformin hydrochloride ER", "product_id": "72789-106_4af6702a-f722-1549-e063-6294a90a6615", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72789-106", "generic_name": "Metformin hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin hydrochloride", "brand_name_suffix": "ER", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA207427", "marketing_category": "ANDA", "marketing_start_date": "20180628", "listing_expiration_date": "20271231"}