atenolol
Generic: atenolol
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
atenolol
Generic Name
atenolol
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
atenolol 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-765
Product ID
43063-765_414b8e3f-9bc8-52f4-e063-6294a90a0eb3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074056
Listing Expiration
2026-12-31
Marketing Start
1995-02-22
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063765
Hyphenated Format
43063-765
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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 (source: ndc)
Generic Name
atenolol (source: ndc)
Application Number
ANDA074056 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-765-30)
- 90 TABLET in 1 BOTTLE, PLASTIC (43063-765-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "414b8e3f-9bc8-52f4-e063-6294a90a0eb3", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0343063765906"], "unii": ["50VV3VW0TI"], "rxcui": ["197381"], "spl_set_id": ["c69b8e5e-c7c3-4883-9cea-f7f435a8ede8"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-765-30)", "package_ndc": "43063-765-30", "marketing_start_date": "20170511"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-765-90)", "package_ndc": "43063-765-90", "marketing_start_date": "20171218"}], "brand_name": "Atenolol", "product_id": "43063-765_414b8e3f-9bc8-52f4-e063-6294a90a0eb3", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "43063-765", "generic_name": "Atenolol", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol", "active_ingredients": [{"name": "ATENOLOL", "strength": "50 mg/1"}], "application_number": "ANDA074056", "marketing_category": "ANDA", "marketing_start_date": "19950222", "listing_expiration_date": "20261231"}