Package 42708-082-21

Brand: benzonatate

Generic: benzonatate
NDC Package Sample

Package Facts

Identity

Package NDC 42708-082-21
Digits Only 4270808221
Product NDC 42708-082
Description

21 CAPSULE in 1 BOTTLE (42708-082-21)

Marketing

Marketing Status
Marketed Since 2019-02-28
Brand benzonatate
Generic benzonatate
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4682a652-1196-5854-e063-6394a90a4c30", "openfda": {"nui": ["N0000009010", "N0000175796"], "unii": ["5P4DHS6ENR"], "rxcui": ["283417"], "spl_set_id": ["55c4ae18-3e37-4caf-9fdb-9d307970b5f9"], "pharm_class_pe": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]"], "pharm_class_epc": ["Non-narcotic Antitussive [EPC]"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "21 CAPSULE in 1 BOTTLE (42708-082-21)", "package_ndc": "42708-082-21", "marketing_start_date": "20190228"}], "brand_name": "BENZONATATE", "product_id": "42708-082_4682a652-1196-5854-e063-6394a90a4c30", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Tracheobronchial Stretch Receptor Activity [PE]", "Non-narcotic Antitussive [EPC]"], "product_ndc": "42708-082", "generic_name": "BENZONATATE", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BENZONATATE", "active_ingredients": [{"name": "BENZONATATE", "strength": "200 mg/1"}], "application_number": "ANDA040627", "marketing_category": "ANDA", "marketing_start_date": "20170322", "listing_expiration_date": "20261231"}