atenolol and chlorthalidone
Generic: atenolol and chlorthalidone
Labeler: ani pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
atenolol and chlorthalidone
Generic Name
atenolol and chlorthalidone
Labeler
ani pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
atenolol 50 mg/1, chlorthalidone 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70954-390
Product ID
70954-390_1dade55e-a8a5-4e38-8ad7-9caa4ceb0cd0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215560
Listing Expiration
2026-12-31
Marketing Start
2021-10-25
Pharmacologic Class
Established (EPC)
Mechanism of Action
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70954390
Hyphenated Format
70954-390
Supplemental Identifiers
RxCUI
UPC
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
atenolol and chlorthalidone (source: ndc)
Generic Name
atenolol and chlorthalidone (source: ndc)
Application Number
ANDA215560 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
- 25 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (70954-390-10)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1dade55e-a8a5-4e38-8ad7-9caa4ceb0cd0", "openfda": {"nui": ["N0000175359", "N0000175420", "N0000000161", "N0000175556"], "upc": ["0370954390107", "0370954391104"], "unii": ["Q0MQD1073Q", "50VV3VW0TI"], "rxcui": ["197382", "197383"], "spl_set_id": ["33690cc7-fffc-4620-888d-7f6453fe58c1"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]", "beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70954-390-10)", "package_ndc": "70954-390-10", "marketing_start_date": "20211025"}], "brand_name": "Atenolol and Chlorthalidone", "product_id": "70954-390_1dade55e-a8a5-4e38-8ad7-9caa4ceb0cd0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70954-390", "generic_name": "Atenolol and Chlorthalidone", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol and Chlorthalidone", "active_ingredients": [{"name": "ATENOLOL", "strength": "50 mg/1"}, {"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA215560", "marketing_category": "ANDA", "marketing_start_date": "20211025", "listing_expiration_date": "20261231"}