Package 68788-7607-5

Brand: benzonatate

Generic: benzonatate
NDC Package

Package Facts

Identity

Package NDC 68788-7607-5
Digits Only 6878876075
Product NDC 68788-7607
Description

15 CAPSULE in 1 BOTTLE (68788-7607-5)

Marketing

Marketing Status
Marketed Since 2020-02-07
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": "f93ea879-5dfe-4175-8980-00437a96f015", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["197397"], "spl_set_id": ["3309040d-e240-42f6-9c51-5c54604a3896"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "9 CAPSULE in 1 BOTTLE (68788-7607-0)", "package_ndc": "68788-7607-0", "marketing_start_date": "20200207"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68788-7607-1)", "package_ndc": "68788-7607-1", "marketing_start_date": "20200207"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE (68788-7607-2)", "package_ndc": "68788-7607-2", "marketing_start_date": "20200207"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-7607-3)", "package_ndc": "68788-7607-3", "marketing_start_date": "20200207"}, {"sample": false, "description": "40 CAPSULE in 1 BOTTLE (68788-7607-4)", "package_ndc": "68788-7607-4", "marketing_start_date": "20200207"}, {"sample": false, "description": "15 CAPSULE in 1 BOTTLE (68788-7607-5)", "package_ndc": "68788-7607-5", "marketing_start_date": "20200207"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (68788-7607-9)", "package_ndc": "68788-7607-9", "marketing_start_date": "20200207"}], "brand_name": "Benzonatate", "product_id": "68788-7607_f93ea879-5dfe-4175-8980-00437a96f015", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "68788-7607", "generic_name": "Benzonatate", "labeler_name": "Preferred Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benzonatate", "active_ingredients": [{"name": "BENZONATATE", "strength": "100 mg/1"}], "application_number": "ANDA206948", "marketing_category": "ANDA", "marketing_start_date": "20200207", "listing_expiration_date": "20261231"}