Package 0480-3309-01

Brand: theophylline

Generic: theophylline
NDC Package

Package Facts

Identity

Package NDC 0480-3309-01
Digits Only 0480330901
Product NDC 0480-3309
Product ID 0480-3309_287dcdda-ce6b-4949-bf12-4316f1f4fe00
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0480-3309-01)

Marketing

Marketing Status
Marketed Since 2023-01-27
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": "287dcdda-ce6b-4949-bf12-4316f1f4fe00", "openfda": {"unii": ["C137DTR5RG"], "rxcui": ["314241", "317769"], "spl_set_id": ["25eabefa-518b-4030-9b72-01ac8b3deba9"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0480-3309-01)", "package_ndc": "0480-3309-01", "marketing_start_date": "20230127"}], "brand_name": "Theophylline", "product_id": "0480-3309_287dcdda-ce6b-4949-bf12-4316f1f4fe00", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "0480-3309", "generic_name": "Theophylline", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Theophylline", "active_ingredients": [{"name": "THEOPHYLLINE", "strength": "450 mg/1"}], "application_number": "ANDA216961", "marketing_category": "ANDA", "marketing_start_date": "20230127", "listing_expiration_date": "20261231"}