metoprolol tartrate and hydrochlorothiazide (27241-301)

Drug Facts

Product Profile

Brand Name metoprolol tartrate and hydrochlorothiazide

Generic Name metoprolol tartrate and hydrochlorothiazide

Labeler ajanta pharma usa inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 25 mg/1, metoprolol tartrate 50 mg/1

Manufacturer

Ajanta Pharma USA Inc.

Identifiers & Regulatory

Product NDC 27241-301

Product ID 27241-301_c1d86752-98ac-48af-8023-e57b40270660

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA215789

Listing Expiration 2026-12-31

Marketing Start 2025-03-15

Pharmacologic Class

Established (EPC)

thiazide diuretic [epc]

Chemical Structure

thiazides [cs]

Physiologic Effect

increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 27241301

Hyphenated Format 27241-301

Supplemental Identifiers

RxCUI

866479 866482

UNII

0J48LPH2TH W5S57Y3A5L

NUI

N0000175359 N0000175419 M0471776

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 metoprolol tartrate and hydrochlorothiazide (source: ndc)

Generic Name metoprolol tartrate and hydrochlorothiazide (source: ndc)

Application Number ANDA215789 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
50 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (27241-301-01)

source: ndc

Packages (1)

27241-301-01 100 TABLET in 1 BOTTLE (27241-301-01)

Ingredients (2)

hydrochlorothiazide (25 mg/1) metoprolol tartrate (50 mg/1)

Linked Drug Pages (1)

METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "c1d86752-98ac-48af-8023-e57b40270660", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "W5S57Y3A5L"], "rxcui": ["866479", "866482"], "spl_set_id": ["8b78d7ad-22a8-4a9f-afb5-d18f0a4e6d36"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (27241-301-01)", "package_ndc": "27241-301-01", "marketing_start_date": "20250315"}], "brand_name": "METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE", "product_id": "27241-301_c1d86752-98ac-48af-8023-e57b40270660", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "27241-301", "generic_name": "metoprolol tartrate and hydrochlorothiazide", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA215789", "marketing_category": "ANDA", "marketing_start_date": "20250315", "listing_expiration_date": "20261231"}