metoprolol tartrate and hydrochlorothiazide
Generic: metoprolol tartrate and hydrochlorothiazide
Labeler: ajanta pharma usa inc.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
Active Ingredients
hydrochlorothiazide 25 mg/1, metoprolol tartrate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
27241-302
Product ID
27241-302_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)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
27241302
Hyphenated Format
27241-302
Supplemental Identifiers
RxCUI
UNII
NUI
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
metoprolol tartrate and hydrochlorothiazide (source: ndc)
Generic Name
metoprolol tartrate and hydrochlorothiazide (source: ndc)
Application Number
ANDA215789 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
- 100 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (27241-302-01)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
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 (27241-302-01)", "package_ndc": "27241-302-01", "marketing_start_date": "20250315"}], "brand_name": "METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE", "product_id": "27241-302_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": "27241-302", "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": "100 mg/1"}], "application_number": "ANDA215789", "marketing_category": "ANDA", "marketing_start_date": "20250315", "listing_expiration_date": "20261231"}