metformin hydrochloride
Generic: metformin hydrochloride
Labeler: camber pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride
Labeler
camber pharmaceuticals, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
metformin hydrochloride 500 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
31722-042
Product ID
31722-042_320180cd-22d3-03bc-e063-6394a90ac74d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215008
Listing Expiration
2026-12-31
Marketing Start
2025-03-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
31722042
Hyphenated Format
31722-042
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
ANDA215008 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/5mL
Packaging
- 1 BOTTLE in 1 CARTON (31722-042-47) / 473 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "320180cd-22d3-03bc-e063-6394a90ac74d", "openfda": {"upc": ["0331722042475"], "unii": ["786Z46389E"], "rxcui": ["861025"], "spl_set_id": ["7cc02a26-5c22-445b-ad8f-3e7570c143d3"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (31722-042-47) / 473 mL in 1 BOTTLE", "package_ndc": "31722-042-47", "marketing_start_date": "20250313"}], "brand_name": "Metformin Hydrochloride", "product_id": "31722-042_320180cd-22d3-03bc-e063-6394a90ac74d", "dosage_form": "SOLUTION", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "31722-042", "generic_name": "Metformin Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/5mL"}], "application_number": "ANDA215008", "marketing_category": "ANDA", "marketing_start_date": "20250313", "listing_expiration_date": "20261231"}