Package 70771-1782-1
Brand: theophylline
Generic: theophyllinePackage Facts
Identity
Package NDC
70771-1782-1
Digits Only
7077117821
Product NDC
70771-1782
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1782-1)
Marketing
Marketing Status
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": "86fdabb8-c881-4695-8127-59b26998e365", "openfda": {"nui": ["N0000175790", "M0023046"], "unii": ["0I55128JYK"], "rxcui": ["314241", "317769"], "spl_set_id": ["7339f98d-b996-4e20-a7a7-315fd2a9fa4d"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_epc": ["Methylxanthine [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1782-1)", "package_ndc": "70771-1782-1", "marketing_start_date": "20240525"}], "brand_name": "Theophylline", "product_id": "70771-1782_86fdabb8-c881-4695-8127-59b26998e365", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "70771-1782", "generic_name": "Theophylline", "labeler_name": "Zydus Lifesciences Limited", "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"}