Package 72578-173-01

Brand: theophylline

Generic: theophylline
NDC Package

Package Facts

Identity

Package NDC 72578-173-01
Digits Only 7257817301
Product NDC 72578-173
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-173-01)

Marketing

Marketing Status
Marketed Since 2024-05-25
Brand theophylline
Generic theophylline
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1e5a0f45-86aa-498a-9cc3-9f7acc210ed6", "openfda": {"nui": ["N0000175790", "M0023046"], "unii": ["0I55128JYK"], "rxcui": ["314241", "317769"], "spl_set_id": ["abdfb9b9-9402-4761-9347-8eb1c4d86242"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_epc": ["Methylxanthine [EPC]"], "manufacturer_name": ["Viona Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-173-01)", "package_ndc": "72578-173-01", "marketing_start_date": "20240525"}], "brand_name": "Theophylline", "product_id": "72578-173_1e5a0f45-86aa-498a-9cc3-9f7acc210ed6", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "72578-173", "generic_name": "Theophylline", "labeler_name": "Viona Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Theophylline", "active_ingredients": [{"name": "THEOPHYLLINE ANHYDROUS", "strength": "300 mg/1"}], "application_number": "ANDA218063", "marketing_category": "ANDA", "marketing_start_date": "20240525", "listing_expiration_date": "20261231"}