atenolol and chlorthalidone

Generic: atenolol and chlorthalidone

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

Drug Facts

Product Profile

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

atenolol 100 mg/1, chlorthalidone 25 mg/1

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 70710-1168
Product ID 70710-1168_f3604313-4dc9-49c1-911c-6178d9939f84
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210028
Listing Expiration 2026-12-31
Marketing Start 2019-03-12

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 707101168
Hyphenated Format 70710-1168

Supplemental Identifiers

RxCUI
197382 197383
UPC
0370710116811 0370710116712
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 ANDA210028 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70710-1168-1)
source: ndc

Packages (1)

70710-1168-1 100 TABLET in 1 BOTTLE (70710-1168-1)

Ingredients (2)

atenolol (100 mg/1) chlorthalidone (25 mg/1)

Linked Drug Pages (1)

Atenolol and Chlorthalidone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f3604313-4dc9-49c1-911c-6178d9939f84", "openfda": {"nui": ["N0000175359", "N0000175420", "N0000000161", "N0000175556"], "upc": ["0370710116811", "0370710116712"], "unii": ["Q0MQD1073Q", "50VV3VW0TI"], "rxcui": ["197382", "197383"], "spl_set_id": ["69131547-f554-4980-b54e-007afc2c696e"], "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": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70710-1168-1)", "package_ndc": "70710-1168-1", "marketing_start_date": "20190312"}], "brand_name": "Atenolol and Chlorthalidone", "product_id": "70710-1168_f3604313-4dc9-49c1-911c-6178d9939f84", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70710-1168", "generic_name": "Atenolol and Chlorthalidone", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol and Chlorthalidone", "active_ingredients": [{"name": "ATENOLOL", "strength": "100 mg/1"}, {"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA210028", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}