Package 72789-442-01

Brand: theophylline

Generic: theophylline
NDC Package

Package Facts

Identity

Package NDC 72789-442-01
Digits Only 7278944201
Product NDC 72789-442
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-442-01)

Marketing

Marketing Status
Marketed Since 2024-10-16
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": "4124d48a-f225-330f-e063-6394a90a8376", "openfda": {"nui": ["N0000175790", "M0023046"], "upc": ["0372789442013"], "unii": ["0I55128JYK"], "rxcui": ["314241"], "spl_set_id": ["5e64036a-ee3e-42e7-9e59-881f88a4e298"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_epc": ["Methylxanthine [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-442-01)", "package_ndc": "72789-442-01", "marketing_start_date": "20241016"}], "brand_name": "Theophylline", "product_id": "72789-442_4124d48a-f225-330f-e063-6394a90a8376", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "72789-442", "generic_name": "Theophylline", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Theophylline", "active_ingredients": [{"name": "THEOPHYLLINE ANHYDROUS", "strength": "450 mg/1"}], "application_number": "ANDA215312", "marketing_category": "ANDA", "marketing_start_date": "20240927", "listing_expiration_date": "20261231"}