Package 72162-1316-1

Brand: benzonatate

Generic: benzonatate
NDC Package

Package Facts

Identity

Package NDC 72162-1316-1
Digits Only 7216213161
Product NDC 72162-1316
Description

100 CAPSULE in 1 BOTTLE (72162-1316-1)

Marketing

Marketing Status
Marketed Since 2023-08-29
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": "01c4f415-1f2d-413b-8696-85aec7791fac", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["283417"], "spl_set_id": ["da093b5e-83a7-467e-9716-bc5827a18c20"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-1316-1)", "package_ndc": "72162-1316-1", "marketing_start_date": "20230829"}], "brand_name": "Benzonatate", "product_id": "72162-1316_01c4f415-1f2d-413b-8696-85aec7791fac", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "72162-1316", "generic_name": "Benzonatate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benzonatate", "active_ingredients": [{"name": "BENZONATATE", "strength": "200 mg/1"}], "application_number": "ANDA211518", "marketing_category": "ANDA", "marketing_start_date": "20190222", "listing_expiration_date": "20261231"}