Package 71993-265-30

Brand: quazepam

Generic: quazepam
NDC Package

Package Facts

Identity

Package NDC 71993-265-30
Digits Only 7199326530
Product NDC 71993-265
Description

30 TABLET in 1 BOTTLE (71993-265-30)

Marketing

Marketing Status
Marketed Since 2018-03-20
Brand quazepam
Generic quazepam
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41da82ab-fab6-7eba-e063-6394a90a037e", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0371993265302"], "unii": ["JF8V0828ZI"], "rxcui": ["198183"], "spl_set_id": ["f7d63f3f-5303-48ab-bce2-35fd62c45799"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Atland Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71993-265-30)", "package_ndc": "71993-265-30", "marketing_start_date": "20180320"}], "brand_name": "Quazepam", "product_id": "71993-265_41da82ab-fab6-7eba-e063-6394a90a037e", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71993-265", "dea_schedule": "CIV", "generic_name": "Quazepam", "labeler_name": "Atland Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quazepam", "active_ingredients": [{"name": "QUAZEPAM", "strength": "15 mg/1"}], "application_number": "NDA018708", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20180320", "listing_expiration_date": "20261231"}