Package 76420-804-01

Brand: benzonatate

Generic: benzonatate
NDC Package

Package Facts

Identity

Package NDC 76420-804-01
Digits Only 7642080401
Product NDC 76420-804
Description

100 CAPSULE in 1 BOTTLE (76420-804-01)

Marketing

Marketing Status
Marketed Since 2024-04-29
Brand benzonatate
Generic benzonatate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3306a754-a59a-d003-e063-6294a90a65c9", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["197397", "283417"], "spl_set_id": ["25ed5206-b322-486f-9e54-14125f6e74c5"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (76420-804-01)", "package_ndc": "76420-804-01", "marketing_start_date": "20240429"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (76420-804-05)", "package_ndc": "76420-804-05", "marketing_start_date": "20240429"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE (76420-804-20)", "package_ndc": "76420-804-20", "marketing_start_date": "20250418"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (76420-804-30)", "package_ndc": "76420-804-30", "marketing_start_date": "20240429"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (76420-804-60)", "package_ndc": "76420-804-60", "marketing_start_date": "20240429"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (76420-804-90)", "package_ndc": "76420-804-90", "marketing_start_date": "20240429"}], "brand_name": "Benzonatate", "product_id": "76420-804_3306a754-a59a-d003-e063-6294a90a65c9", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "76420-804", "generic_name": "Benzonatate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benzonatate", "active_ingredients": [{"name": "BENZONATATE", "strength": "200 mg/1"}], "application_number": "ANDA206948", "marketing_category": "ANDA", "marketing_start_date": "20181221", "listing_expiration_date": "20261231"}