metformin hydrochloride

Generic: metformin hydrochloride

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metformin hydrochloride
Generic Name metformin hydrochloride
Labeler camber pharmaceuticals, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

metformin hydrochloride 500 mg/5mL

Manufacturer
Camber Pharmaceuticals, Inc.

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
biguanide [epc] biguanides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722042
Hyphenated Format 31722-042

Supplemental Identifiers

RxCUI
861025
UPC
0331722042475
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 (source: ndc)
Application Number ANDA215008 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (31722-042-47) / 473 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

metformin hydrochloride (500 mg/5mL)

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"}