Package 69452-267-20

Brand: theophylline

Generic: theophylline
NDC Package

Package Facts

Identity

Package NDC 69452-267-20
Digits Only 6945226720
Product NDC 69452-267
Product ID 69452-267_07895277-4273-508f-e063-6394a90a40ea
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69452-267-20)

Marketing

Marketing Status
Marketed Since 2023-10-12
Brand theophylline
Generic theophylline
Sample Package No

Linked Drug Pages (1)

Theophylline ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "07895277-4273-508f-e063-6394a90a40ea", "openfda": {"nui": ["N0000175790", "M0023046"], "unii": ["0I55128JYK"], "rxcui": ["317769"], "spl_set_id": ["63517422-45a0-4e78-8505-eca054068ee9"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_epc": ["Methylxanthine [EPC]"], "manufacturer_name": ["Bionpharma Inc.,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69452-267-20)", "package_ndc": "69452-267-20", "marketing_start_date": "20231012"}], "brand_name": "Theophylline", "product_id": "69452-267_07895277-4273-508f-e063-6394a90a40ea", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "69452-267", "generic_name": "Theophylline", "labeler_name": "Bionpharma Inc.,", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Theophylline", "active_ingredients": [{"name": "THEOPHYLLINE ANHYDROUS", "strength": "300 mg/1"}], "application_number": "ANDA216300", "marketing_category": "ANDA", "marketing_start_date": "20231012", "listing_expiration_date": "20261231"}