metolazone

Generic: metolazone

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

Drug Facts

Product Profile

Brand Name metolazone
Generic Name metolazone
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

metolazone 10 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-534
Product ID 62332-534_4e197913-c368-474d-a147-e9ade3021e37
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213251
Listing Expiration 2026-12-31
Marketing Start 2020-12-02

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 62332534
Hyphenated Format 62332-534

Supplemental Identifiers

RxCUI
197978 197979 311671
UPC
0362332534319 0362332533312 0362332532315
UNII
TZ7V40X7VX
NUI
N0000175359 N0000175420

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 metolazone (source: ndc)
Generic Name metolazone (source: ndc)
Application Number ANDA213251 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (62332-534-31)
  • 1000 TABLET in 1 BOTTLE (62332-534-91)
source: ndc

Packages (2)

Ingredients (1)

metolazone (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4e197913-c368-474d-a147-e9ade3021e37", "openfda": {"nui": ["N0000175359", "N0000175420"], "upc": ["0362332534319", "0362332533312", "0362332532315"], "unii": ["TZ7V40X7VX"], "rxcui": ["197978", "197979", "311671"], "spl_set_id": ["a84dbb37-648e-42d4-8688-ac39599284f0"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62332-534-31)", "package_ndc": "62332-534-31", "marketing_start_date": "20201202"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62332-534-91)", "package_ndc": "62332-534-91", "marketing_start_date": "20201202"}], "brand_name": "METOLAZONE", "product_id": "62332-534_4e197913-c368-474d-a147-e9ade3021e37", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "62332-534", "generic_name": "METOLAZONE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOLAZONE", "active_ingredients": [{"name": "METOLAZONE", "strength": "10 mg/1"}], "application_number": "ANDA213251", "marketing_category": "ANDA", "marketing_start_date": "20201202", "listing_expiration_date": "20261231"}