Package 72789-231-15

Brand: benzonatate

Generic: benzonatate
NDC Package

Package Facts

Identity

Package NDC 72789-231-15
Digits Only 7278923115
Product NDC 72789-231
Description

15 CAPSULE in 1 BOTTLE, PLASTIC (72789-231-15)

Marketing

Marketing Status
Marketed Since 2022-02-08
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": "2d6c8ca3-bf6c-22a9-e063-6294a90a2029", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["197397"], "spl_set_id": ["55b64aee-d4c4-4aad-9016-0dd879e979e6"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 CAPSULE in 1 BOTTLE, PLASTIC (72789-231-15)", "package_ndc": "72789-231-15", "marketing_start_date": "20220208"}], "brand_name": "Benzonatate", "product_id": "72789-231_2d6c8ca3-bf6c-22a9-e063-6294a90a2029", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "72789-231", "generic_name": "Benzonatate", "labeler_name": "PD-Rx 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": "20181221", "listing_expiration_date": "20261231"}