metolazone

Generic: metolazone

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metolazone
Generic Name metolazone
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metolazone 5 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7329
Product ID 0904-7329_59f5dd79-a3de-41e1-8ae3-f3fd67fcc3e8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213827
Marketing Start 2023-08-30
Marketing End 2026-08-31

Pharmacologic Class

Established (EPC)
thiazide-like diuretic [epc]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047329
Hyphenated Format 0904-7329

Supplemental Identifiers

RxCUI
197979 311671
UNII
TZ7V40X7VX
NUI
N0000175359 N0000175420

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 metolazone (source: ndc)
Generic Name metolazone (source: ndc)
Application Number ANDA213827 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7329-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

metolazone (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "59f5dd79-a3de-41e1-8ae3-f3fd67fcc3e8", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["TZ7V40X7VX"], "rxcui": ["197979", "311671"], "spl_set_id": ["8e8bbe58-0845-40d1-9831-82435f01c7be"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7329-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7329-61", "marketing_end_date": "20260831", "marketing_start_date": "20230830"}], "brand_name": "Metolazone", "product_id": "0904-7329_59f5dd79-a3de-41e1-8ae3-f3fd67fcc3e8", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "0904-7329", "generic_name": "Metolazone", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metolazone", "active_ingredients": [{"name": "METOLAZONE", "strength": "5 mg/1"}], "application_number": "ANDA213827", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20230830"}