atenolol and chlorthalidone

Generic: atenolol and chlorthalidone

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

Drug Facts

Product Profile

Brand Name atenolol and chlorthalidone
Generic Name atenolol and chlorthalidone
Labeler ani pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 50 mg/1, chlorthalidone 25 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

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)
thiazide-like diuretic [epc] beta-adrenergic blocker [epc]
Mechanism of Action
adrenergic beta-antagonists [moa]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70954390
Hyphenated Format 70954-390

Supplemental Identifiers

RxCUI
197382 197383
UPC
0370954390107 0370954391104
UNII
Q0MQD1073Q 50VV3VW0TI
NUI
N0000175359 N0000175420 N0000000161 N0000175556

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 atenolol and chlorthalidone (source: ndc)
Generic Name atenolol and chlorthalidone (source: ndc)
Application Number ANDA215560 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70954-390-10)
source: ndc

Packages (1)

Ingredients (2)

atenolol (50 mg/1) chlorthalidone (25 mg/1)

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"}