Package 42858-701-01
Brand: theophylline anhydrous
Generic: theophyllinePackage Facts
Identity
Package NDC
42858-701-01
Digits Only
4285870101
Product NDC
42858-701
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42858-701-01)
Marketing
Marketing Status
Brand
theophylline anhydrous
Generic
theophylline
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5bbaf151-7dc4-4860-9e46-a2e85071c120", "openfda": {"nui": ["N0000175790", "M0023046"], "unii": ["0I55128JYK"], "rxcui": ["313291"], "spl_set_id": ["bba266d2-1d22-49a9-b3db-e4f06802a8a9"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_epc": ["Methylxanthine [EPC]"], "manufacturer_name": ["Rhodes Pharmaceuticals L.P."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42858-701-01)", "package_ndc": "42858-701-01", "marketing_start_date": "20120202"}], "brand_name": "Theophylline Anhydrous", "product_id": "42858-701_5bbaf151-7dc4-4860-9e46-a2e85071c120", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "42858-701", "generic_name": "Theophylline", "labeler_name": "Rhodes Pharmaceuticals L.P.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Theophylline", "brand_name_suffix": "Anhydrous", "active_ingredients": [{"name": "THEOPHYLLINE ANHYDROUS", "strength": "400 mg/1"}], "application_number": "ANDA040086", "marketing_category": "ANDA", "marketing_start_date": "20120202", "listing_expiration_date": "20261231"}