atenolol and chlorthalidone
Generic: atenolol and chlorthalidone
Labeler: unichem pharmaceuticals (usa), inc.Drug Facts
Product Profile
Brand Name
atenolol and chlorthalidone
Generic Name
atenolol and chlorthalidone
Labeler
unichem pharmaceuticals (usa), inc.
Dosage Form
TABLET
Routes
Active Ingredients
atenolol 100 mg/1, chlorthalidone 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
29300-401
Product ID
29300-401_383b2bb2-513e-4bcf-8fc7-32c0cda3481e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213302
Listing Expiration
2026-12-31
Marketing Start
2020-11-25
Pharmacologic Class
Established (EPC)
Mechanism of Action
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
29300401
Hyphenated Format
29300-401
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
atenolol and chlorthalidone (source: ndc)
Generic Name
atenolol and chlorthalidone (source: ndc)
Application Number
ANDA213302 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
- 25 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (29300-401-01)
- 500 TABLET in 1 BOTTLE (29300-401-05)
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "383b2bb2-513e-4bcf-8fc7-32c0cda3481e", "openfda": {"nui": ["N0000175359", "N0000175420", "N0000000161", "N0000175556"], "unii": ["Q0MQD1073Q", "50VV3VW0TI"], "rxcui": ["197382", "197383"], "spl_set_id": ["a85d28c1-e812-4c12-aa67-136bff3610e5"], "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": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (29300-401-01)", "package_ndc": "29300-401-01", "marketing_start_date": "20201214"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (29300-401-05)", "package_ndc": "29300-401-05", "marketing_start_date": "20201214"}], "brand_name": "Atenolol and Chlorthalidone", "product_id": "29300-401_383b2bb2-513e-4bcf-8fc7-32c0cda3481e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "29300-401", "generic_name": "Atenolol and Chlorthalidone", "labeler_name": "Unichem 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": "ANDA213302", "marketing_category": "ANDA", "marketing_start_date": "20201125", "listing_expiration_date": "20261231"}