Package 68462-356-05

Brand: theophylline

Generic: theophylline
NDC Package

Package Facts

Identity

Package NDC 68462-356-05
Digits Only 6846235605
Product NDC 68462-356
Product ID 68462-356_7c8e32e3-ca36-4ad2-971b-446c12a81992
Description

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-356-05)

Marketing

Marketing Status
Marketed Since 2010-07-13
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": "7c8e32e3-ca36-4ad2-971b-446c12a81992", "openfda": {"nui": ["N0000175790", "M0023046"], "upc": ["0368462380017", "0368462356012"], "unii": ["0I55128JYK"], "rxcui": ["313291", "348472"], "spl_set_id": ["56fc2167-ceb6-4e3e-8ff7-5e400dfbd533"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_epc": ["Methylxanthine [EPC]"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-356-01)", "package_ndc": "68462-356-01", "marketing_start_date": "20100713"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-356-05)", "package_ndc": "68462-356-05", "marketing_start_date": "20100713"}], "brand_name": "Theophylline", "product_id": "68462-356_7c8e32e3-ca36-4ad2-971b-446c12a81992", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "68462-356", "generic_name": "Theophylline", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Theophylline", "active_ingredients": [{"name": "THEOPHYLLINE ANHYDROUS", "strength": "600 mg/1"}], "application_number": "ANDA090355", "marketing_category": "ANDA", "marketing_start_date": "20100713", "listing_expiration_date": "20271231"}