Package 31722-078-01

Brand: theophylline

Generic: theophylline
NDC Package

Package Facts

Identity

Package NDC 31722-078-01
Digits Only 3172207801
Product NDC 31722-078
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-078-01)

Marketing

Marketing Status
Marketed Since 2023-09-08
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": "05c7eb1d-0b79-ee46-e063-6294a90abfe4", "openfda": {"nui": ["N0000175790", "M0023046"], "unii": ["0I55128JYK"], "rxcui": ["314241", "317769"], "spl_set_id": ["bf320619-c53b-49a7-97b5-cd0c075a9f75"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_epc": ["Methylxanthine [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-078-01)", "package_ndc": "31722-078-01", "marketing_start_date": "20230908"}], "brand_name": "Theophylline", "product_id": "31722-078_05c7eb1d-0b79-ee46-e063-6294a90abfe4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "31722-078", "generic_name": "Theophylline", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Theophylline", "active_ingredients": [{"name": "THEOPHYLLINE ANHYDROUS", "strength": "450 mg/1"}], "application_number": "ANDA217422", "marketing_category": "ANDA", "marketing_start_date": "20230908", "listing_expiration_date": "20261231"}