Package 67296-2202-3

Brand: benzonatate

Generic: benzonatate
NDC Package

Package Facts

Identity

Package NDC 67296-2202-3
Digits Only 6729622023
Product NDC 67296-2202
Description

30 CAPSULE, LIQUID FILLED in 1 BOTTLE (67296-2202-3)

Marketing

Marketing Status
Marketed Since 2024-09-29
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": "46e97552-8f98-7fd1-e063-6394a90a3c92", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["283417"], "spl_set_id": ["46e97547-23d9-114a-e063-6394a90a920b"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, LIQUID FILLED in 1 BOTTLE (67296-2202-3)", "package_ndc": "67296-2202-3", "marketing_start_date": "20240929"}], "brand_name": "Benzonatate", "product_id": "67296-2202_46e97552-8f98-7fd1-e063-6394a90a3c92", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "67296-2202", "generic_name": "Benzonatate", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benzonatate", "active_ingredients": [{"name": "BENZONATATE", "strength": "200 mg/1"}], "application_number": "ANDA040682", "marketing_category": "ANDA", "marketing_start_date": "20240929", "listing_expiration_date": "20261231"}